A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036842



Internal ID19126061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:24049660..24092083hg38UCSC Ensembl
Innerchr10:24338589..24381012hg19UCSC Ensembl
Innerchr10:24378595..24421018hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3842424
hg1942424
hg1842424
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv688n100
Supporting Variantsnssv3505522
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)nsv1036842
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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