A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181796



Internal ID20748836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18404782..18425937hg38UCSC Ensembl
chr11:18426329..18447484hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3821156
hg1921156
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441684
Supporting Variants
Samples
Known GenesLDHA, LDHC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181796
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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