A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054555



Internal ID18797086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1515950..1922951hg38UCSC Ensembl
Innerchr10:1558145..1965145hg19UCSC Ensembl
Innerchr10:1548145..1955145hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38407002
hg19407001
hg18407001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3496812
Samples
Known GenesADARB2, ADARB2-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054555
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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