A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997819



Internal ID19157356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:165541222..165592958hg38UCSC Ensembl
Innerchr3:165259010..165310746hg19UCSC Ensembl
Innerchr3:166741704..166793440hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3851737
hg1951737
hg1851737
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4974n100
Supporting Variantsnssv3612589, nssv3612590, nssv3612588
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)nsv997819
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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