A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1077181



Internal ID15930367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167935400..168196562hg38UCSC Ensembl
Innerchr6:168336080..168597242hg19UCSC Ensembl
Innerchr6:168078929..168340091hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38261163
hg19261163
hg18261163
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605387
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)nssv1077181
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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