A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3506076



Internal ID18457671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46287904hg38UCSC Ensembl
Innerchr10:47541177..47659140hg19UCSC Ensembl
Innerchr10:47011183..47129146hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38117964
hg19117964
hg18117964
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036342
Supporting Variants
Samples
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3506076
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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