A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524910



Internal ID20898271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9397994..9398997hg38UCSC Ensembl
chr18:9397992..9398995hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg381004
hg191004
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044381
Samples
Known GenesTWSG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524910
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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