A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192045



Internal ID20759085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91406301..91410200hg38UCSC Ensembl
chr10:93166058..93169957hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg383900
hg193900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443471
Supporting Variants
Samples
Known GenesLOC100188947
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192045
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0002


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