A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17558227



Internal ID21882582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:91212024..91212024hg38UCSC Ensembl
chr7:90841339..90841339hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6069635
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17558227
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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