A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054062



Internal ID19143281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:56569449..56725241hg38UCSC Ensembl
Innerchr10:58329209..58485001hg19UCSC Ensembl
Innerchr10:57999215..58155007hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38155793
hg19155793
hg18155793
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv869n100
Supporting Variantsnssv3516471
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)nsv1054062
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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