A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670285



Internal ID15406937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35170884..35189099hg38UCSC Ensembl
Innerchr19:35661787..35680002hg19UCSC Ensembl
Innerchr19:40353627..40371842hg18UCSC Ensembl
Innerchr19:40353627..40371842hg17UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3818216
hg1918216
hg1818216
hg1718216
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516540
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv670285
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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