A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16895910



Internal ID171436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15085472..15091431hg38UCSC Ensembl
chr1:15411968..15417927hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg385960
hg195960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415681
Supporting Variants
Samples
Known GenesKAZN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16895910
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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