A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091999



Internal ID22001232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28168026..28168026hg38UCSC Ensembl
chr17:26495052..26495052hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628632
Samples
Known GenesNLK
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091999
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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