A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997732



Internal ID18810582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:93308..148728hg38UCSC Ensembl
Innerchr3:134991..190411hg19UCSC Ensembl
Innerchr3:109991..165411hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3855421
hg1955421
hg1855421
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3590263
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)nsv997732
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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