A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1154919



Internal ID15854070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167935400..168198653hg38UCSC Ensembl
Innerchr6:168336080..168599333hg19UCSC Ensembl
Innerchr6:168078929..168342182hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38263254
hg19263254
hg18263254
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605388
Supporting Variants
Samples1780854556_A
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)nssv1154919
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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