A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983212



Internal ID18271720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:122685001..122695304hg38UCSC Ensembl
Innerchr11:122555709..122566012hg19UCSC Ensembl
Innerchr11:122060919..122071222hg18UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3810304
hg1910304
hg1810304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2758811
SamplesHGDP00778
Known GenesUBASH3B
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv983212
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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