A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635529



Internal ID7022328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101556228..101557976hg38UCSC Ensembl
Innerchr14:101556276..101557929hg38UCSC Ensembl
Outerchr14:101556181..101558024hg38UCSC Ensembl
chr14:102022565..102024313hg19UCSC Ensembl
Innerchr14:102022613..102024266hg19UCSC Ensembl
Outerchr14:102022518..102024361hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg381749
hg191749
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15108809, essv15108810
SamplesHG02061, HG02060
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635529
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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