A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1008566



Internal ID15955836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:144088649..144114635hg38UCSC Ensembl
Innerchr4:145009802..145035788hg19UCSC Ensembl
Innerchr4:145229252..145255238hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3825987
hg1925987
hg1825987
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595618
Supporting Variants
Samples
Known GenesGYPA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1008566
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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