A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053112



Internal ID19142331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34464502..34545554hg38UCSC Ensembl
Innerchr10:34753430..34834482hg19UCSC Ensembl
Innerchr10:34793436..34874488hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3881053
hg1981053
hg1881053
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3521515
Samples
Known GenesPARD3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053112
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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