A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17381868



Internal ID22439738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88710822..88712976hg38UCSC Ensembl
chr15:89254053..89256207hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382155
hg192155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5944368
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17381868
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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