A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17041767



Internal ID95551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7217172..7217248hg38UCSC Ensembl
chr11:7238403..7238479hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6143608
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17041767
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00125


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