A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054503



Internal ID19143722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:65838083..65895842hg38UCSC Ensembl
Innerchr10:67597841..67655600hg19UCSC Ensembl
Innerchr10:67267847..67325606hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3857760
hg1957760
hg1857760
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3522193
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)nsv1054503
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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