A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517376



Internal ID15444669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:50757732..50777499hg38UCSC Ensembl
Innerchr19:51260989..51280756hg19UCSC Ensembl
Innerchr19:55952801..55972568hg18UCSC Ensembl
Innerchr19:55952801..55972568hg17UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3819768
hg1919768
hg1819768
hg1719768
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv681781, nssv690724, nssv676639, nssv667682, nssv676550, nssv651844, nssv702230, nssv657536, nssv692313, nssv692514, nssv670754, nssv666694
Samples
Known GenesGPR32
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517376
Frequency
Sample Size2026
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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