A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18197002



Internal ID20764042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99705769..99817324hg38UCSC Ensembl
chr15:100245974..100357529hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38111556
hg19111556
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514419
Supporting Variants
Samples
Known GenesDNM1P46, LYSMD4, MEF2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18197002
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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