A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998608



Internal ID18811458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4139709..4221511hg38UCSC Ensembl
Innerchr3:4181393..4263195hg19UCSC Ensembl
Innerchr3:4156393..4238195hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3881803
hg1981803
hg1881803
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4654n100
Supporting Variantsnssv3591620
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)nsv998608
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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