A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050993



Internal ID19140212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3398272..3591901hg38UCSC Ensembl
Innerchr11:3419502..3613131hg19UCSC Ensembl
Innerchr11:3376078..3569707hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38193630
hg19193630
hg18193630
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1018n100
Supporting Variantsnssv3521892, nssv3503979
Samples
Known GenesLOC650368
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050993
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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