A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16282784



Internal ID20492002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77261609..77307976hg38UCSC Ensembl
chr7:76890926..76937293hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3846368
hg1946368
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4748332
Supporting Variants
Samples
Known GenesCCDC146
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16282784
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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