A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999075



Internal ID18811925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46761415..46805739hg38UCSC Ensembl
Innerchr3:46802905..46847229hg19UCSC Ensembl
Innerchr3:46777909..46822233hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3844325
hg1944325
hg1844325
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4736n100
Supporting Variantsnssv3593801, nssv3593800
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)nsv999075
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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