A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008088



Internal ID19097307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:161698314..161831189hg38UCSC Ensembl
Innerchr3:161416102..161548977hg19UCSC Ensembl
Innerchr3:162898796..163031671hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38132876
hg19132876
hg18132876
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4931n100
Supporting Variantsnssv3606419, nssv3606413, nssv3606414, nssv3741564, nssv3606416, nssv3606418, nssv3741562, nssv3606411, nssv3606420, nssv3606417, nssv3606412, nssv3741563, nssv3606415
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)nsv1008088
Frequency
Sample Size11257
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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