A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522341



Internal ID15449634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:45136866..45160960hg38UCSC Ensembl
Innerchr19:45640124..45664218hg19UCSC Ensembl
Innerchr19:50331964..50356058hg18UCSC Ensembl
Innerchr19:50331964..50356058hg17UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3824095
hg1924095
hg1824095
hg1724095
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695120
Samples
Known GenesNKPD1, PPP1R37
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522341
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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