A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1077131



Internal ID15930317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167930255..168208655hg38UCSC Ensembl
Innerchr6:168330935..168609335hg19UCSC Ensembl
Innerchr6:168073784..168352184hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38278401
hg19278401
hg18278401
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605372
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)nssv1077131
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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