A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16895871



Internal ID171407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:14969899..14987425hg38UCSC Ensembl
chr1:15296395..15313921hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3817527
hg1917527
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557565
Supporting Variants
Samples
Known GenesKAZN
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16895871
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000937


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