A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17561809



Internal ID21886164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:68258609..68258734hg38UCSC Ensembl
chr7:67723596..67723721hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6012769
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17561809
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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