A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567816



Internal ID20940887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:604326..1858568hg38UCSC Ensembl
chr5:604441..1858682hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg381254243
hg191254242
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5585n223
Supporting Variantsnssv18268936
Samples
Known GenesBRD9, CEP72, CLPTM1L, LOC100506688, LOC100996325, LOC101929034, LOC728613, LPCAT1, MIR4277, MIR4457, MIR4635, MIR6075, MRPL36, NDUFS6, NKD2, SDHAP3, SLC12A7, SLC6A18, SLC6A19, SLC6A3, TERT, TPPP, TRIP13, ZDHHC11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567816
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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