A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5467595



Internal ID245405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:62621919..62621999hg38UCSC Ensembl
chr4:63487637..63487717hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16950207
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5467595
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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