A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5455708



Internal ID233785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174496965..174511818hg38UCSC Ensembl
chr4:175418116..175432969hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3814854
hg1914854
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16959355
Samples
Known GenesHPGD
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5455708
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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