A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17484176



Internal ID22542084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44262257..44266141hg38UCSC Ensembl
chr22:44658137..44662021hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg383885
hg193885
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5882840
Supporting Variants
Samples
Known GenesKIAA1644
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17484176
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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