A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053485



Internal ID18796016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46195678..46286428hg38UCSC Ensembl
Innerchr10:47566914..47657664hg19UCSC Ensembl
Innerchr10:47036920..47127670hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3890751
hg1990751
hg1890751
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv840n100
Supporting Variantsnssv3522512
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)nsv1053485
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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