A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16952367



Internal ID35603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:76709018..76726256hg38UCSC Ensembl
chr4:77630171..77647409hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg3817239
hg1917239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467192
Supporting Variants
Samples
Known GenesSHROOM3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16952367
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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