A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003642



Internal ID19092860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176202710..176280832hg38UCSC Ensembl
Innerchr3:175920498..175998620hg19UCSC Ensembl
Innerchr3:177403192..177481314hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3878123
hg1978123
hg1878123
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4993n100
Supporting Variantsnssv3614950, nssv3738448
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)nsv1003642
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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