A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17636577



Internal ID21828624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18892390..18892532hg38UCSC Ensembl
chr19:19003199..19003341hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042776
Supporting Variants
Samples
Known GenesCERS1, GDF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17636577
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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