A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702695



Internal ID15439347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:51505937..51511906hg38UCSC Ensembl
Innerchr6:51370735..51376704hg19UCSC Ensembl
Innerchr6:51478694..51484663hg18UCSC Ensembl
Innerchr6:51478694..51484663hg17UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg385970
hg195970
hg185970
hg175970
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526396
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702695
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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