A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16895982



Internal ID171478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15187497..15193921hg38UCSC Ensembl
chr1:15513993..15520417hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg386425
hg196425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5426254
Supporting Variants
Samples
Known GenesTMEM51
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16895982
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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