A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634877



Internal ID7021677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71363310..71377094hg38UCSC Ensembl
Innerchr14:71363338..71377067hg38UCSC Ensembl
Outerchr14:71363283..71377122hg38UCSC Ensembl
chr14:71830027..71843811hg19UCSC Ensembl
Innerchr14:71830055..71843784hg19UCSC Ensembl
Outerchr14:71830000..71843839hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3813785
hg1913785
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15053936, essv15053937, essv15053935, essv15053938
SamplesNA19819, NA19113, NA19435, HG02053
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634877
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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