A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv681120



Internal ID15071086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43155365..43158934hg38UCSC Ensembl
Innerchr19:43659517..43663086hg19UCSC Ensembl
Innerchr19:48351357..48354926hg18UCSC Ensembl
Innerchr19:48351357..48354926hg17UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg383570
hg193570
hg183570
hg173570
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516973
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv681120
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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