A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5432225



Internal ID210974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:14763163..14765194hg38UCSC Ensembl
chr1:15089659..15091690hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg382032
hg192032
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16897064
Samples
Known GenesKAZN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5432225
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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