A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012722



Internal ID19101939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:22101754..22208250hg38UCSC Ensembl
Innerchr2:22324626..22431122hg19UCSC Ensembl
Innerchr2:22178131..22284627hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38106497
hg19106497
hg18106497
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3579011
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)nsv1012722
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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