A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038805



Internal ID19128024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:24083364..24102024hg38UCSC Ensembl
Innerchr10:24372293..24390953hg19UCSC Ensembl
Innerchr10:24412299..24430959hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3818661
hg1918661
hg1818661
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv689n100
Supporting Variantsnssv3510455
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)nsv1038805
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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