A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572251



Internal ID20945322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:142844217..142844594hg38UCSC Ensembl
chr5:142223782..142224159hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38378
hg19378
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266285
Samples
Known GenesARHGAP26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572251
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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