A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18024867



Internal ID20591907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55874737..55900912hg38UCSC Ensembl
chr15:56166935..56193110hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3826176
hg1926176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496412
Supporting Variants
Samples
Known GenesNEDD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18024867
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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