A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522811



Internal ID15103418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:39514000..39517580hg38UCSC Ensembl
Innerchr19:40004640..40008220hg19UCSC Ensembl
Innerchr19:44696480..44700060hg18UCSC Ensembl
Innerchr19:44696480..44700060hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg383581
hg193581
hg183581
hg173581
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698457
Samples
Known GenesSELV
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522811
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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