A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004464



Internal ID18746995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46770667..46805739hg38UCSC Ensembl
Innerchr3:46812157..46847229hg19UCSC Ensembl
Innerchr3:46787161..46822233hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3835073
hg1935073
hg1835073
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4736n100
Supporting Variantsnssv3595228
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)nsv1004464
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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