A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178554



Internal ID20745594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132224778..132352220hg38UCSC Ensembl
chr10:134038282..134165724hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38127443
hg19127443
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453027
Supporting Variants
Samples
Known GenesLRRC27, STK32C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178554
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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