A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17382236



Internal ID22440106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65305702..65309176hg38UCSC Ensembl
chr15:65598040..65601514hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg383475
hg193475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5932549
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17382236
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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