A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639876



Internal ID7026654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7979463..7980830hg38UCSC Ensembl
Innerchr17:7979463..7980830hg38UCSC Ensembl
Outerchr17:7979261..7980963hg38UCSC Ensembl
chr17:7882781..7884148hg19UCSC Ensembl
Innerchr17:7882781..7884148hg19UCSC Ensembl
Outerchr17:7882579..7884281hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381368
hg191368
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15605437, essv15605434, essv15605435, essv15605433, essv15605436
SamplesNA20321, NA20320, NA19317, HG02511, NA19467
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639876
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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