A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087942



Internal ID21997175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30897128..30897128hg38UCSC Ensembl
chr13:31471265..31471265hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602535
Samples
Known GenesTEX26-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087942
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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