A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181451



Internal ID20748491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132293463..132358347hg38UCSC Ensembl
chr10:134106967..134171851hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3864885
hg1964885
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6455509
Supporting Variants
Samples
Known GenesLRRC27, STK32C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181451
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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