A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18025695



Internal ID20592735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64765074..64769943hg38UCSC Ensembl
chr15:65057273..65062142hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg384870
hg194870
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6510035
Supporting Variants
Samples
Known GenesRBPMS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18025695
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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