A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571267



Internal ID20944338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:140685442..140686081hg38UCSC Ensembl
chr5:140065027..140065666hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38640
hg19640
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267508
Samples
Known GenesHARS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571267
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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