A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562421



Internal ID335376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:73761764..73762887hg38UCSC Ensembl
chr2:73988891..73990014hg19UCSC Ensembl
Cytoband2p13.1
Allele length
AssemblyAllele length
hg381124
hg191124
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16915480
Samples
Known GenesDUSP11
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562421
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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