A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287114



Internal ID20496332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:91584049..91590556hg38UCSC Ensembl
chr7:91213364..91219871hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg386508
hg196508
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4745874
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287114
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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