A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18027159



Internal ID20594199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83023662..83028178hg38UCSC Ensembl
chr15:83692414..83696930hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg384517
hg194517
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6507193
Supporting Variants
Samples
Known GenesBTBD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18027159
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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