A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035512



Internal ID19124731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:24086322..24096443hg38UCSC Ensembl
Innerchr10:24375251..24385372hg19UCSC Ensembl
Innerchr10:24415257..24425378hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3810122
hg1910122
hg1810122
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3503857
Samples
Known GenesKIAA1217
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035512
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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