A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035398



Internal ID18777929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46304297hg38UCSC Ensembl
Innerchr10:47541177..47675533hg19UCSC Ensembl
Innerchr10:47011183..47145539hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38134357
hg19134357
hg18134357
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv833n100
Supporting Variantsnssv3505900, nssv3509132
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)nsv1035398
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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