A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17735112



Internal ID158778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:69834594..69835973hg38UCSC Ensembl
chr4:70700312..70701691hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg381380
hg191380
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5456132
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17735112
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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