A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5510283



Internal ID286907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76961784..76966865hg38UCSC Ensembl
chr11:76672828..76677909hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg385082
hg195082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17047236
Samples
Known GenesACER3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5510283
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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