A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17576926



Internal ID21768969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:145614399..145643393hg38UCSC Ensembl
chr6:145935535..145964529hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg3828995
hg1928995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6011261
Supporting Variants
Samples
Known GenesEPM2A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17576926
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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