A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584192



Internal ID20957263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:19549581..21274519hg38UCSC Ensembl
chr13:20123721..21848658hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg381724939
hg191724938
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1762n223
Supporting Variantsnssv18235334
Samples
Known GenesCRYL1, GJA3, GJB2, GJB6, IFT88, IL17D, LATS2, LINC00367, MIR4499, MPHOSPH8, MRP63, N6AMT2, PSPC1, SAP18, SKA3, TPTE2, XPO4, ZMYM2, ZMYM5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584192
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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