A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638677



Internal ID7025462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55002970..55027662hg38UCSC Ensembl
Innerchr16:55002976..55027656hg38UCSC Ensembl
Outerchr16:55002964..55027668hg38UCSC Ensembl
chr16:55036882..55061574hg19UCSC Ensembl
Innerchr16:55036888..55061568hg19UCSC Ensembl
Outerchr16:55036876..55061580hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3824693
hg1924693
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15480937
SamplesHG00099
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638677
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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