A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17627131



Internal ID21819178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17006225..17014168hg38UCSC Ensembl
chr19:17117035..17124978hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg387944
hg197944
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042957
Supporting Variants
Samples
Known GenesCPAMD8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17627131
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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