A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050683



Internal ID18793214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46176448..46290653hg38UCSC Ensembl
Innerchr10:47547684..47661889hg19UCSC Ensembl
Innerchr10:47017690..47131895hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38114206
hg19114206
hg18114206
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv833n100
Supporting Variantsnssv3517201
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)nsv1050683
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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