A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668141



Internal ID15058107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167935400..168195571hg38UCSC Ensembl
Innerchr6:168336080..168596251hg19UCSC Ensembl
Innerchr6:168078929..168339100hg18UCSC Ensembl
Innerchr6:168154636..168414807hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38260172
hg19260172
hg18260172
hg17260172
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515568
Supporting Variants
Samples
Known GenesFRMD1, HGC6.3, KIF25, KIF25-AS1, MLLT4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668141
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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