A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553830



Internal ID20926943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44201019..44242711hg38UCSC Ensembl
chr22:44596899..44638591hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3841693
hg1941693
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207545
Samples
Known GenesPARVG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553830
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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