A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280884



Internal ID20490102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157048060..157048133hg38UCSC Ensembl
chr7:156840754..156840827hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4733915
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280884
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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