A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595516



Internal ID16382925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:135732439..135788675hg38UCSC Ensembl
Innerchr4:136653594..136709830hg19UCSC Ensembl
Innerchr4:136873044..136929280hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3856237
hg1956237
hg1856237
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153510
SamplesHGDP00863
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595516
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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