A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702520



Internal ID15092486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:55793241..55795036hg38UCSC Ensembl
Innerchr19:56304607..56306402hg19UCSC Ensembl
Innerchr19:60996419..60998214hg18UCSC Ensembl
Innerchr19:60996419..60998214hg17UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg381796
hg191796
hg181796
hg171796
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526248
Supporting Variants
Samples
Known GenesNLRP11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702520
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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