A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17688414



Internal ID112080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77572345..77575984hg38UCSC Ensembl
chr11:77283390..77287029hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg383640
hg193640
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5497830
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17688414
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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