A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595609



Internal ID16383018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:143947855..144009062hg38UCSC Ensembl
Innerchr4:144869008..144930215hg19UCSC Ensembl
Innerchr4:145088458..145149665hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3861208
hg1961208
hg1861208
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1008562
Samples
Known GenesGYPB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595609
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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