A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592041



Internal ID20965112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:27547839..27548681hg38UCSC Ensembl
chr17:25874865..25875707hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38843
hg19843
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241605
Samples
Known GenesKSR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592041
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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