A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545018



Internal ID15985741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1638499..1688102hg38UCSC Ensembl
Innerchr1:1573861..1619541hg19UCSC Ensembl
Innerchr1:1563724..1609404hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3849604
hg1945681
hg1845681
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv708605
Samples
Known GenesCDK11B, SLC35E2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545018
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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