A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044891



Internal ID19134110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:24083828..24106218hg38UCSC Ensembl
Innerchr10:24372757..24395147hg19UCSC Ensembl
Innerchr10:24412763..24435153hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3822391
hg1922391
hg1822391
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv691n100
Supporting Variantsnssv3511396
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)nsv1044891
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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