A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002091



Internal ID19091308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176202710..176282539hg38UCSC Ensembl
Innerchr3:175920498..176000327hg19UCSC Ensembl
Innerchr3:177403192..177483021hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3879830
hg1979830
hg1879830
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4993n100
Supporting Variantsnssv3614951, nssv3614953, nssv3614952
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)nsv1002091
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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