A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17388657



Internal ID22446527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65326077..65326472hg38UCSC Ensembl
chr15:65618415..65618810hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5941129
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17388657
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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