A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035322



Internal ID19124541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:62377308..62497169hg38UCSC Ensembl
Innerchr10:64137067..64256928hg19UCSC Ensembl
Innerchr10:63807073..63926934hg18UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38119862
hg19119862
hg18119862
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3503637
Samples
Known GenesZNF365
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035322
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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