A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16897064



Internal ID172195
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 StatusS
Merged Variantsnsv5432225
Supporting Variants
Samples
Known GenesKAZN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16897064
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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