A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15191657



Internal ID21330518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:77520178..77520178hg38UCSC Ensembl
chr10:79279936..79279936hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3931843
Supporting Variants
SamplesHG002
Known GenesKCNMA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15191657
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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