A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516606



Internal ID15443899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:121421420..121475851hg38UCSC Ensembl
Innerchr4:122342575..122397006hg19UCSC Ensembl
Innerchr4:122562025..122616456hg18UCSC Ensembl
Innerchr4:122700180..122754611hg17UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3854432
hg1954432
hg1854432
hg1754432
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv689942, nssv701451, nssv669516, nssv680051, nssv688228, nssv672934, nssv673092
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516606
Frequency
Sample Size2026
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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