A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053832



Internal ID19143051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:54262437..54301840hg38UCSC Ensembl
Innerchr10:56022197..56061600hg19UCSC Ensembl
Innerchr10:55692203..55731606hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3839404
hg1939404
hg1839404
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3520272
Samples
Known GenesPCDH15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053832
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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