A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18024898



Internal ID20591938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56370901..56541500hg38UCSC Ensembl
chr15:56663099..56833698hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38170600
hg19170600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497078
Supporting Variants
Samples
Known GenesMNS1, TEX9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18024898
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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