A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696856



Internal ID15433508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:103822858..103855928hg38UCSC Ensembl
Innerchr6:104270733..104303803hg19UCSC Ensembl
Innerchr6:104377426..104410496hg18UCSC Ensembl
Innerchr6:104377426..104410496hg17UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3833071
hg1933071
hg1833071
hg1733071
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519440
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696856
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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