A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18139432



Internal ID20706472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134495825..134502548hg38UCSC Ensembl
chr6:134816963..134823686hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg386724
hg196724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619052
Supporting Variants
Samples
Known GenesLINC01010
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18139432
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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