A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16277940



Internal ID20487158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107888700..107888818hg38UCSC Ensembl
chr7:107529145..107529263hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4748403
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16277940
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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