A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521477



Internal ID15102084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:48673773..48693829hg38UCSC Ensembl
Innerchr19:49177030..49197086hg19UCSC Ensembl
Innerchr19:53868842..53888898hg18UCSC Ensembl
Innerchr19:53868842..53888898hg17UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3820057
hg1920057
hg1820057
hg1720057
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698089
Samples
Known GenesSEC1P
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521477
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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