A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003997



Internal ID19093214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162153428..162235787hg38UCSC Ensembl
Innerchr3:161871216..161953575hg19UCSC Ensembl
Innerchr3:163353910..163436269hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3882360
hg1982360
hg1882360
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4932n100
Supporting Variantsnssv3607917, nssv3607918
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)nsv1003997
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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