A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180814



Internal ID20747854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22753601..22786500hg38UCSC Ensembl
chr15:23086568..23119509hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3832900
hg1932942
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6510040
Supporting Variants
Samples
Known GenesLOC283683, NIPA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180814
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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