A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697264



Internal ID15087230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:92795097..92796691hg38UCSC Ensembl
Innerchr6:93504815..93506409hg19UCSC Ensembl
Innerchr6:93561536..93563130hg18UCSC Ensembl
Innerchr6:93561536..93563130hg17UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg381595
hg191595
hg181595
hg171595
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517329
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697264
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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