A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17482962



Internal ID22540868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39063222..39068653hg38UCSC Ensembl
chr22:39459227..39464658hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg385432
hg195432
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5874416
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17482962
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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