A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17395178



Internal ID22453048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29440170..29441904hg38UCSC Ensembl
chr19:29931077..29932811hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg381735
hg191735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5932762
Supporting Variants
Samples
Known GenesLOC284395
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17395178
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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