A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17041708



Internal ID95512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6691113..6703658hg38UCSC Ensembl
chr11:6712344..6724889hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3812546
hg1912546
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5500800
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17041708
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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