A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5554887



Internal ID328058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:97123296..97580178hg38UCSC Ensembl
chr2:97789033..98196641hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38456883
hg19407609
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16916990
Samples
Known GenesANKRD36, ANKRD36B, LOC100506076, LOC100506123
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5554887
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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