A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587456



Internal ID20960527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:52409512..53222775hg38UCSC Ensembl
chr17:50486872..51300136hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38813264
hg19813265
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245246
Samples
Known GenesC17orf112
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587456
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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