A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16286854



Internal ID20496072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:73137237..73137357hg38UCSC Ensembl
chr17:71133376..71133496hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4746875
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16286854
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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