A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091844



Internal ID22001077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5511996..5511996hg38UCSC Ensembl
chr17:5415316..5415316hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17629036
Samples
Known GenesNLRP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091844
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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