A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634965



Internal ID7021765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75474031..75477924hg38UCSC Ensembl
Innerchr14:75474032..75477924hg38UCSC Ensembl
Outerchr14:75474031..75477925hg38UCSC Ensembl
chr14:75940734..75944627hg19UCSC Ensembl
Innerchr14:75940735..75944627hg19UCSC Ensembl
Outerchr14:75940734..75944628hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg383894
hg193894
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15064352, essv15064346, essv15064351, essv15064347, essv15064350, essv15064348, essv15064349, essv15064354, essv15064345, essv15064344, essv15064355, essv15064353
SamplesNA20317, NA19917, HG02623, HG03055, NA20318, HG02442, HG02439, HG03476, HG01444, HG03419, HG03084, HG02629
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634965
Frequency
Sample Size2504
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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