A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007905



Internal ID19097124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:83785283..83928958hg38UCSC Ensembl
Innerchr2:84012407..84156082hg19UCSC Ensembl
Innerchr2:83865918..84009593hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38143676
hg19143676
hg18143676
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3582165
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)nsv1007905
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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