A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189258



Internal ID20756298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86755201..86757700hg38UCSC Ensembl
chr10:88514958..88517457hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6435905
Supporting Variants
Samples
Known GenesBMPR1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189258
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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