A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1077216



Internal ID15930402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167942096..168177248hg38UCSC Ensembl
Innerchr6:168342776..168577928hg19UCSC Ensembl
Innerchr6:168085625..168320777hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38235153
hg19235153
hg18235153
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605402
Supporting Variants
Samples
Known GenesFRMD1, HGC6.3, KIF25, KIF25-AS1, MLLT4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1077216
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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