A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635202



Internal ID7022001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:85734690..85738553hg38UCSC Ensembl
Innerchr14:85734691..85738553hg38UCSC Ensembl
Outerchr14:85734690..85738554hg38UCSC Ensembl
chr14:86201034..86204897hg19UCSC Ensembl
Innerchr14:86201035..86204897hg19UCSC Ensembl
Outerchr14:86201034..86204898hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg383864
hg193864
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15089811, essv15089805, essv15089789, essv15089809, essv15089784, essv15089778, essv15089808, essv15089802, essv15089794, essv15089804, essv15089799, essv15089786, essv15089777, essv15089806, essv15089783, essv15089775, essv15089779, essv15089797, essv15089796, essv15089791, essv15089792, essv15089798, essv15089807, essv15089785, essv15089812, essv15089776, essv15089780, essv15089801, essv15089795, essv15089787, essv15089781, essv15089793, essv15089788, essv15089814, essv15089790, essv15089803, essv15089782, essv15089810, essv15089800, essv15089813
SamplesHG03484, HG01356, HG03378, HG02433, HG02419, HG02012, NA20298, NA19393, HG01971, HG03577, NA18519, HG03086, HG03385, HG03189, HG02573, NA19207, NA19901, NA19239, NA19707, HG02554, HG02450, HG03123, HG02881, HG02256, NA19225, NA19318, HG02586, HG02675, HG02722, HG02772, HG00734, HG02314, NA19835, HG02274, HG03351, HG02768, NA19102, NA19312, HG03303, HG02343
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635202
Frequency
Sample Size2504
Observed Gain0
Observed Loss40
Observed Complex0
Frequencyn/a


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