A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267559



Internal ID20476777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76046294..76046350hg38UCSC Ensembl
chr7:75675612..75675668hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4734412
Supporting Variants
Samples
Known GenesSTYXL1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267559
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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