A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056479



Internal ID19145698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:9949277..10081421hg38UCSC Ensembl
Innerchr18:9949274..10081418hg19UCSC Ensembl
Innerchr18:9939274..10071418hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38132145
hg19132145
hg18132145
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3725289
Samples
Known GenesVAPA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056479
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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