A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009581



Internal ID19098799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:2797812..2925450hg38UCSC Ensembl
Innerchr1:2714377..2842015hg19UCSC Ensembl
Innerchr1:2704237..2831875hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38127639
hg19127639
hg18127639
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12n100
Supporting Variantsnssv3467767
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)nsv1009581
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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