A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008651



Internal ID19097868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:35244401..35671420hg38UCSC Ensembl
Innerchr2:35469467..35896486hg19UCSC Ensembl
Innerchr2:35322971..35749990hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38427020
hg19427020
hg18427020
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3581137
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)nsv1008651
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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