A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594986



Internal ID20968057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28051080..28051471hg38UCSC Ensembl
chr17:26378106..26378497hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38392
hg19392
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241619
Samples
Known GenesNLK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594986
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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