A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638778



Internal ID7025563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:61579289..61585740hg38UCSC Ensembl
Innerchr16:61579289..61585740hg38UCSC Ensembl
Outerchr16:61579071..61586043hg38UCSC Ensembl
chr16:61613193..61619644hg19UCSC Ensembl
Innerchr16:61613193..61619644hg19UCSC Ensembl
Outerchr16:61612975..61619947hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg386452
hg196452
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15496284
SamplesHG00174
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638778
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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