A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183334



Internal ID20750374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132341083..132400255hg38UCSC Ensembl
chr10:134154587..134213759hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3859173
hg1959173
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439750
Supporting Variants
Samples
Known GenesLRRC27, PWWP2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183334
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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