A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699315



Internal ID15089281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:188150854..188174086hg38UCSC Ensembl
Innerchr4:189072008..189095240hg19UCSC Ensembl
Innerchr4:189309002..189332234hg18UCSC Ensembl
Innerchr4:189447157..189470389hg17UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3823233
hg1923233
hg1823233
hg1723233
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519300
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699315
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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