A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006018



Internal ID19095236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:40877389..40910816hg38UCSC Ensembl
Innerchr1:41343061..41376488hg19UCSC Ensembl
Innerchr1:41115648..41149075hg18UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3833428
hg1933428
hg1833428
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv154n100
Supporting Variantsnssv3482022
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)nsv1006018
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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