A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701349



Internal ID15091315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:190137954..190141334hg38UCSC Ensembl
Innerchr3:189855743..189859123hg19UCSC Ensembl
Innerchr3:191338437..191341817hg18UCSC Ensembl
Innerchr3:191338445..191341825hg17UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg383381
hg193381
hg183381
hg173381
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525254
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701349
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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