A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703816



Internal ID15093782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:58355068..58385345hg38UCSC Ensembl
Innerchr19:58866434..58896712hg19UCSC Ensembl
Innerchr19:63558246..63588524hg18UCSC Ensembl
Innerchr19:63558246..63588524hg17UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3830278
hg1930279
hg1830279
hg1730279
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515731
Supporting Variants
Samples
Known GenesA1BG-AS1, ZNF497, ZNF837
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703816
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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