A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17725221



Internal ID148887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44260447..44260759hg38UCSC Ensembl
chr19:44764600..44764912hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5528443
Supporting Variants
Samples
Known GenesZNF233
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17725221
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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