A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705999



Internal ID15442651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:114919221..115077995hg38UCSC Ensembl
Innerchr6:115240385..115399159hg19UCSC Ensembl
Innerchr6:115347078..115505852hg18UCSC Ensembl
Innerchr6:115347078..115505852hg17UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38158775
hg19158775
hg18158775
hg17158775
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522607
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705999
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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