A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517436



Internal ID15098043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14135617..14187630hg38UCSC Ensembl
Innerchr19:14246429..14298442hg19UCSC Ensembl
Innerchr19:14107429..14159442hg18UCSC Ensembl
Innerchr19:14107429..14159442hg17UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3852014
hg1952014
hg1852014
hg1752014
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv678216, nssv652016, nssv667027, nssv686292, nssv689705, nssv683127, nssv669114
Samples
Known GenesASF1B, LOC100507373, LPHN1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517436
Frequency
Sample Size2026
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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