A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635413



Internal ID7022212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96061027..96069365hg38UCSC Ensembl
Innerchr14:96061028..96069365hg38UCSC Ensembl
Outerchr14:96061027..96069366hg38UCSC Ensembl
chr14:96527364..96535702hg19UCSC Ensembl
Innerchr14:96527365..96535702hg19UCSC Ensembl
Outerchr14:96527364..96535703hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg388339
hg198339
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15103432, essv15103431, essv15103427, essv15103425, essv15103429, essv15103430, essv15103426, essv15103428
SamplesHG03175, NA19190, HG03209, HG02508, HG03027, HG02497, HG01915, HG03303
Known GenesC14orf132
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635413
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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