A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17588002



Internal ID21780045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:58545338..58545338hg38UCSC Ensembl
chr10:60305098..60305098hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6095781
Supporting Variants
Samples
Known GenesBICC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17588002
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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