A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700915



Internal ID15437567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:87947803..87947934hg38UCSC Ensembl
Innerchr4:88868955..88869086hg19UCSC Ensembl
Innerchr4:89087979..89088110hg18UCSC Ensembl
Innerchr4:89226134..89226265hg17UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38132
hg19132
hg18132
hg17132
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524904
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700915
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer