A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15197005



Internal ID21335801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3310321..3310380hg38UCSC Ensembl
chr6:3310555..3310614hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3944425
Supporting Variants
SamplesHG002
Known GenesSLC22A23
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15197005
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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