A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005022



Internal ID19094239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:79485089..79641217hg38UCSC Ensembl
Innerchr1:79950774..80106902hg19UCSC Ensembl
Innerchr1:79723362..79879490hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38156129
hg19156129
hg18156129
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3472411
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)nsv1005022
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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