A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3504997



Internal ID18456592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46293101hg38UCSC Ensembl
Innerchr10:47541177..47664337hg19UCSC Ensembl
Innerchr10:47011183..47134343hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38123161
hg19123161
hg18123161
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054148
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)nssv3504997
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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