A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050531



Internal ID19139750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:96447445..96544562hg38UCSC Ensembl
Innerchr11:96180609..96277727hg19UCSC Ensembl
Innerchr11:95820257..95917375hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3897118
hg1997119
hg1897119
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1255n100
Supporting Variantsnssv3520993
Samples
Known GenesJRKL-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050531
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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