A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588213



Internal ID20961284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:56665226..56666342hg38UCSC Ensembl
chr18:54332457..54333573hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg381117
hg191117
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245339
Samples
Known GenesWDR7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588213
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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