A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3654788



Internal ID18606383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:13419498..13571556hg38UCSC Ensembl
Innerchr6:13419730..13571788hg19UCSC Ensembl
Innerchr6:13527709..13679767hg18UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38152059
hg19152059
hg18152059
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033620
Supporting Variants
Samples
Known GenesGFOD1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3654788
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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