A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091030



Internal ID22000263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76379078..76379078hg38UCSC Ensembl
chr17:74375159..74375159hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622755
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091030
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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