A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583942



Internal ID20957013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76463604..76464336hg38UCSC Ensembl
chr17:74459686..74460418hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38733
hg19733
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243201
Samples
Known GenesAANAT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583942
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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