A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581171



Internal ID20954242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:19051674..20424294hg38UCSC Ensembl
chr13:19625814..20998433hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg381372621
hg191372620
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226464
Samples
Known GenesANKRD26P3, CRYL1, GJA3, GJB2, GJB6, LINC00421, MPHOSPH8, PSPC1, RNU6-52P, TPTE2, TUBA3C, ZMYM2, ZMYM5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581171
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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