A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010896



Internal ID19100113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:15326975..15395739hg38UCSC Ensembl
Innerchr2:15467099..15535863hg19UCSC Ensembl
Innerchr2:15384550..15453314hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3868765
hg1968765
hg1868765
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3577112
Samples
Known GenesNBAS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010896
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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