A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043708



Internal ID19132927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:57070537..57105582hg38UCSC Ensembl
Innerchr10:58830297..58865342hg19UCSC Ensembl
Innerchr10:58500303..58535348hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3835046
hg1935046
hg1835046
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv874n100
Supporting Variantsnssv3507254
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)nsv1043708
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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