A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17390779



Internal ID22448649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18261533..18261766hg38UCSC Ensembl
chr19:18372343..18372576hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5943830
Supporting Variants
Samples
Known GenesKIAA1683
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17390779
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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