A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885835



Internal ID22660821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42004083..42005382hg38UCSC Ensembl
chr22:42400087..42401386hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483550
Samples
Known GenesWBP2NL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885835
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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