A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139326



Internal ID338511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:97515618..97643618hg38UCSC Ensembl
chr2:98132081..98260081hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38128001
hg19128001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16916827
Samples
Known GenesANKRD36B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139326
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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