A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18140121



Internal ID20707161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136269028..136269636hg38UCSC Ensembl
chr6:136590166..136590774hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38609
hg19609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6616367
Supporting Variants
Samples
Known GenesBCLAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18140121
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00011


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