A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560641



Internal ID20933712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76865931..76866182hg38UCSC Ensembl
chr5:76161756..76162007hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270236
Samples
Known GenesS100Z
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560641
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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