A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268989



Internal ID20478207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:148476020..148476098hg38UCSC Ensembl
chr7:148173112..148173190hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4746569
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268989
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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