A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705585



Internal ID15442237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:54425535..54472332hg38UCSC Ensembl
Innerchr6:54290333..54337130hg19UCSC Ensembl
Innerchr6:54398292..54445089hg18UCSC Ensembl
Innerchr6:54398292..54445089hg17UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3846798
hg1946798
hg1846798
hg1746798
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528901
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705585
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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