A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1008562



Internal ID16302518
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 StatusS
Merged Variantsnsv595609
Supporting Variants
Samples
Known GenesGYPB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1008562
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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