A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035647



Internal ID19124866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:126409190..126508964hg38UCSC Ensembl
Innerchr10:128097759..128197533hg19UCSC Ensembl
Innerchr10:128087749..128187523hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3899775
hg1999775
hg1899775
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3706255
Samples
Known GenesC10orf90, LINC00601
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035647
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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