A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654873



Internal ID15044839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167935400..168026466hg38UCSC Ensembl
Innerchr6:168336080..168427146hg19UCSC Ensembl
Innerchr6:168078929..168169995hg18UCSC Ensembl
Innerchr6:168154636..168245702hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3891067
hg1991067
hg1891067
hg1791067
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515568
Supporting Variants
Samples
Known GenesHGC6.3, KIF25, KIF25-AS1, MLLT4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv654873
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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