A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16900043



Internal ID806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19434966..19435206hg38UCSC Ensembl
chr1:19761460..19761700hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5429292
Supporting Variants
Samples
Known GenesCAPZB
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16900043
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.179051


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