A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17407757



Internal ID22465627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45157437..45157749hg38UCSC Ensembl
chr19:45660695..45661007hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5939531
Supporting Variants
Samples
Known GenesNKPD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17407757
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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