A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517555



Internal ID15444848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:87966193..87966961hg38UCSC Ensembl
Innerchr4:88887345..88888113hg19UCSC Ensembl
Innerchr4:89106369..89107137hg18UCSC Ensembl
Innerchr4:89244524..89245292hg17UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38769
hg19769
hg18769
hg17769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv659438, nssv672635, nssv652349
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517555
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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