A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17375121



Internal ID22600790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36341147..36341301hg38UCSC Ensembl
chr15:36633348..36633502hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5931018
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17375121
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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