A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17568094



Internal ID21760137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:115411489..115411489hg38UCSC Ensembl
chr7:115051543..115051543hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg381898
hg191898
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6075480
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17568094
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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