A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191042



Internal ID20758082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113495026..113757564hg38UCSC Ensembl
chr10:115254785..115517323hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38262539
hg19262539
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443022
Supporting Variants
Samples
Known GenesCASP7, HABP2, NRAP, PLEKHS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191042
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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