A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5493955



Internal ID271116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76396593..76400361hg38UCSC Ensembl
chr11:76107637..76111405hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg383769
hg193769
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17048537
Samples
Known GenesLOC100506127
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5493955
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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