A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17397722



Internal ID22455592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2761681..2761896hg38UCSC Ensembl
chr19:2761679..2761894hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5942005
Supporting Variants
Samples
Known GenesSGTA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17397722
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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