A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188193



Internal ID20755233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40530252..40731066hg38UCSC Ensembl
chr15:40822451..41023264hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38200815
hg19200814
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502932
Supporting Variants
Samples
Known GenesC15orf57, CASC5, MRPL42P5, RAD51, RAD51-AS1, RPUSD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188193
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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