A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18023347



Internal ID20590387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34865888..34866495hg38UCSC Ensembl
chr15:35158089..35158696hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38608
hg19608
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502677
Supporting Variants
Samples
Known GenesAQR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18023347
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00024


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