A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3749708



Internal ID18701303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167934598..168204432hg38UCSC Ensembl
Innerchr6:168335278..168605112hg19UCSC Ensembl
Innerchr6:168078127..168347961hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38269835
hg19269835
hg18269835
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030606
Supporting Variants
Samples
Known GenesFRMD1, HGC6.3, KIF25, KIF25-AS1, MLLT4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3749708
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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