A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555581



Internal ID20928666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42385168..42506643hg38UCSC Ensembl
chr22:42781174..42902649hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38121476
hg19121476
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207448
Samples
Known GenesNFAM1, SERHL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555581
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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