A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17377126



Internal ID22434996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59780954..59811649hg38UCSC Ensembl
chr15:60073153..60103848hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3830696
hg1930696
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5944243
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17377126
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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