A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697086



Internal ID15433738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:128606501..128653772hg38UCSC Ensembl
Innerchr4:129527656..129574927hg19UCSC Ensembl
Innerchr4:129747106..129794377hg18UCSC Ensembl
Innerchr4:129885261..129932532hg17UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg3847272
hg1947272
hg1847272
hg1747272
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519852
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697086
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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