A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5446856



Internal ID225174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:223827223..223828878hg38UCSC Ensembl
chr1:224014925..224016580hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg381656
hg191656
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16896340
Samples
Known GenesTP53BP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5446856
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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