A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3749029



Internal ID18700624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10486213..10559867hg38UCSC Ensembl
Innerchr6:10486446..10560100hg19UCSC Ensembl
Innerchr6:10594432..10668086hg18UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3873655
hg1973655
hg1873655
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027649
Supporting Variants
Samples
Known GenesGCNT2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3749029
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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