A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037533



Internal ID19126752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:128243421..128384451hg38UCSC Ensembl
Innerchr10:130041685..130182715hg19UCSC Ensembl
Innerchr10:129931675..130072705hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38141031
hg19141031
hg18141031
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3505074
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037533
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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