A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17393634



Internal ID22451504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:24860911..24860911hg38UCSC Ensembl
chr22:25256878..25256878hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38240
hg19240
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5975317
Supporting Variants
Samples
Known GenesSGSM1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17393634
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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