A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007879



Internal ID19097098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:112112973..112163506hg38UCSC Ensembl
Innerchr1:112655595..112706128hg19UCSC Ensembl
Innerchr1:112457118..112507651hg18UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg3850534
hg1950534
hg1850534
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv282n100
Supporting Variantsnssv3494639
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)nsv1007879
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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