A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701169



Internal ID15437821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:48191092..48198962hg38UCSC Ensembl
Innerchr19:48694349..48702219hg19UCSC Ensembl
Innerchr19:53386161..53394031hg18UCSC Ensembl
Innerchr19:53386161..53394031hg17UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg387871
hg197871
hg187871
hg177871
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525109
Supporting Variants
Samples
Known GenesC19orf68
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701169
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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