A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3506359



Internal ID18457954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46279715hg38UCSC Ensembl
Innerchr10:47541177..47650951hg19UCSC Ensembl
Innerchr10:47011183..47120957hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38109775
hg19109775
hg18109775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053502
Supporting Variants
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)nssv3506359
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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