A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18137757



Internal ID20704797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:12861994..12862573hg38UCSC Ensembl
chr6:12862226..12862805hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg38580
hg19580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411508
Supporting Variants
Samples
Known GenesPHACTR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18137757
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0004


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