A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012630



Internal ID19101847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:80030709..80295512hg38UCSC Ensembl
Innerchr1:80496394..80761197hg19UCSC Ensembl
Innerchr1:80268982..80533785hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38264804
hg19264804
hg18264804
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3473416
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)nsv1012630
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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