A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17401092



Internal ID22458962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3674444..3674593hg38UCSC Ensembl
chr19:3674442..3674591hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5935861
Supporting Variants
Samples
Known GenesPIP5K1C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17401092
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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