A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010213



Internal ID19099431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:144056516..144144307hg38UCSC Ensembl
Innerchr3:143775358..143863149hg19UCSC Ensembl
Innerchr3:145258048..145345839hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3887792
hg1987792
hg1887792
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4914n100
Supporting Variantsnssv3606129, nssv3606130
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)nsv1010213
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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