A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055130



Internal ID18797661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46279306hg38UCSC Ensembl
Innerchr10:47541177..47650542hg19UCSC Ensembl
Innerchr10:47011183..47120548hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38109366
hg19109366
hg18109366
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv831n100
Supporting Variantsnssv3518135
Samples
Known GenesANTXRLP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055130
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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