A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192236



Internal ID20759276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101310845..101668788hg38UCSC Ensembl
chr10:103070602..103428545hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38357944
hg19357944
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443400
Supporting Variants
Samples
Known GenesBTRC, DPCD, FBXW4, MIR3158-1, MIR3158-2, POLL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192236
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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