A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012862



Internal ID19102079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:73340527..73432347hg38UCSC Ensembl
Innerchr1:73806210..73898030hg19UCSC Ensembl
Innerchr1:73578798..73670618hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3891821
hg1991821
hg1891821
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3478500, nssv3479753
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)nsv1012862
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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