A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17047334



Internal ID99401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46359908..46411705hg38UCSC Ensembl
chr11:46381458..46433255hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3851798
hg1951798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5507746
Supporting Variants
Samples
Known GenesAMBRA1, CHRM4, DGKZ, MDK, MIR4688
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17047334
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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