A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5500038



Internal ID276987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61340219..61340598hg38UCSC Ensembl
chr11:61107691..61108070hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38380
hg19380
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17046545
Samples
Known GenesDAK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5500038
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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