A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035359



Internal ID19124578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:57712230..57797870hg38UCSC Ensembl
Innerchr10:59471990..59557630hg19UCSC Ensembl
Innerchr10:59141996..59227636hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3885641
hg1985641
hg1885641
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3707146
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)nsv1035359
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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