A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700702



Internal ID15437354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:39171988..39181364hg38UCSC Ensembl
Innerchr6:39139764..39149140hg19UCSC Ensembl
Innerchr6:39247742..39257118hg18UCSC Ensembl
Innerchr6:39247742..39257118hg17UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg389377
hg199377
hg189377
hg179377
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524717
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700702
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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