A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081165



Internal ID21990398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75777152..75777152hg38UCSC Ensembl
chr17:73773233..73773233hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17630535
Samples
Known GenesH3F3B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081165
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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