A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638840



Internal ID7025625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:64914370..64920504hg38UCSC Ensembl
Innerchr16:64914370..64920504hg38UCSC Ensembl
Outerchr16:64913870..64921004hg38UCSC Ensembl
chr16:64948273..64954407hg19UCSC Ensembl
Innerchr16:64948273..64954407hg19UCSC Ensembl
Outerchr16:64947773..64954907hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg386135
hg196135
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15499377
SamplesNA19390
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638840
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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