A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526232



Internal ID15106839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:50797973..50832687hg38UCSC Ensembl
Innerchr19:51301230..51335943hg19UCSC Ensembl
Innerchr19:55993042..56027755hg18UCSC Ensembl
Innerchr19:55993042..56027755hg17UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3834715
hg1934714
hg1834714
hg1734714
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv203n21
Supporting Variantsnssv702499
Samples
Known GenesC19orf48, KLK1, KLK15, MGC45922, SNORD88A, SNORD88B, SNORD88C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526232
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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