A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044835



Internal ID18787366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:132852920..133019278hg38UCSC Ensembl
Innerchr10:134666424..134832782hg19UCSC Ensembl
Innerchr10:134516414..134682772hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38166359
hg19166359
hg18166359
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv995n100
Supporting Variantsnssv3511341
Samples
Known GenesLOC399829, TTC40
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044835
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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