A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3749558



Internal ID19047839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:145355935..145487312hg38UCSC Ensembl
Innerchr6:145677071..145808448hg19UCSC Ensembl
Innerchr6:145718764..145850141hg18UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38131378
hg19131378
hg18131378
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017166
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3749558
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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