A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551515



Internal ID20924649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44253092..44258265hg38UCSC Ensembl
chr22:44648972..44654145hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg385174
hg195174
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207547
Samples
Known GenesKIAA1644
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551515
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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