A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1077271



Internal ID15930457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167949001..168178987hg38UCSC Ensembl
Innerchr6:168349681..168579667hg19UCSC Ensembl
Innerchr6:168092530..168322516hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38229987
hg19229987
hg18229987
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605434
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)nssv1077271
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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