A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010629



Internal ID19099846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:192516979..192681272hg38UCSC Ensembl
Innerchr2:193381705..193545998hg19UCSC Ensembl
Innerchr2:193089950..193254243hg18UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38164294
hg19164294
hg18164294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4139n100
Supporting Variantsnssv3583909
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)nsv1010629
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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