A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv652016



Internal ID15041982
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517436
Supporting Variants
Samples
Known GenesASF1B, LOC100507373, LPHN1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv652016
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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