A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563681



Internal ID20936752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:82186873..82187272hg38UCSC Ensembl
chr5:81482692..81483091hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269621
Samples
Known GenesATG10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563681
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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