A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637609



Internal ID7024400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1259252..1303571hg38UCSC Ensembl
Innerchr16:1259752..1303071hg38UCSC Ensembl
Outerchr16:1258252..1304571hg38UCSC Ensembl
chr16:1309253..1353572hg19UCSC Ensembl
Innerchr16:1309753..1353072hg19UCSC Ensembl
Outerchr16:1308253..1354572hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3844320
hg1944320
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15359740, essv15359739, essv15359737, essv15359738, essv15359736, essv15359735
SamplesNA18508, NA19020, HG01110, HG03123, NA19035, HG03063
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637609
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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