A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035422



Internal ID18777953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:110964401..111004836hg38UCSC Ensembl
Innerchr10:112724159..112764594hg19UCSC Ensembl
Innerchr10:112714149..112754584hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3840436
hg1940436
hg1840436
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3503733
Samples
Known GenesSHOC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035422
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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