A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260544



Internal ID20469762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158803547..158803604hg38UCSC Ensembl
chr6:159224579..159224636hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4746814
Supporting Variants
Samples
Known GenesEZR
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260544
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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