A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18022788



Internal ID20589828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22855335..22857308hg38UCSC Ensembl
chr15:23015760..23017733hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381974
hg191974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504647
Supporting Variants
Samples
Known GenesNIPA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18022788
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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