A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567414



Internal ID20940485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43135065..43135627hg38UCSC Ensembl
chr5:43135167..43135729hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38563
hg19563
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268385
Samples
Known GenesZNF131
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567414
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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