A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999013



Internal ID19158549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:22747460..22839241hg38UCSC Ensembl
Innerchr3:22788951..22880732hg19UCSC Ensembl
Innerchr3:22763955..22855736hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3891782
hg1991782
hg1891782
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4700n100
Supporting Variantsnssv3589490
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)nsv999013
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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