A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17590247



Internal ID21782290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7939841..7939841hg38UCSC Ensembl
chr11:7961388..7961388hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6095052
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17590247
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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