A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584962



Internal ID20958033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:19190117..21198044hg38UCSC Ensembl
chr13:19764257..21772183hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg382007928
hg192007927
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1762n223
Supporting Variantsnssv18228625
Samples
Known GenesANKRD26P3, CRYL1, GJA3, GJB2, GJB6, IFT88, IL17D, LATS2, LINC00367, LINC00421, MIR4499, MPHOSPH8, MRP63, N6AMT2, PSPC1, SAP18, SKA3, TPTE2, XPO4, ZMYM2, ZMYM5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584962
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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