A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv544956



Internal ID15985679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1171093..1241217hg38UCSC Ensembl
Innerchr1:1106473..1176597hg19UCSC Ensembl
Innerchr1:1096336..1166460hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3870125
hg1970125
hg1870125
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv708518
Samples
Known GenesB3GALT6, SDF4, TNFRSF18, TNFRSF4, TTLL10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv544956
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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