A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17392409



Internal ID22450279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7559802..7560098hg38UCSC Ensembl
chr19:7624688..7624984hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5946984
Supporting Variants
Samples
Known GenesPNPLA6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17392409
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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