A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997463



Internal ID19156999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:185164255..185307689hg38UCSC Ensembl
Innerchr2:186028982..186172416hg19UCSC Ensembl
Innerchr2:185737227..185880661hg18UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38143435
hg19143435
hg18143435
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4124n100
Supporting Variantsnssv3729293
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)nsv997463
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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