A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3749553



Internal ID19047834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:141667329..141753178hg38UCSC Ensembl
Innerchr6:141988466..142074315hg19UCSC Ensembl
Innerchr6:142030159..142116008hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3885850
hg1985850
hg1885850
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024891
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)nssv3749553
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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