A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv685952



Internal ID15075918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167935400..168198653hg38UCSC Ensembl
Innerchr6:168336080..168599333hg19UCSC Ensembl
Innerchr6:168078929..168342182hg18UCSC Ensembl
Innerchr6:168154636..168417889hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38263254
hg19263254
hg18263254
hg17263254
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)nssv685952
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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