A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556923



Internal ID330042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:66526378..66527692hg38UCSC Ensembl
chr2:66753510..66754824hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg381315
hg191315
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16913931
Samples
Known GenesMEIS1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556923
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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