A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550962



Internal ID20924105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41820012..41824540hg38UCSC Ensembl
chr22:42216016..42220544hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg384529
hg194529
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074539
Samples
Known GenesCCDC134
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550962
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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