A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17507562



Internal ID22565510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:139623255..139627061hg38UCSC Ensembl
chr8:140635498..140639304hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg383807
hg193807
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5849333
Supporting Variants
Samples
Known GenesKCNK9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17507562
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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