A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599170



Internal ID20972241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54297101..54577125hg38UCSC Ensembl
chr19:54807711..55088592hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38280025
hg19280882
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3723n223
Supporting Variantsnssv18248453
Samples
Known GenesCDC42EP5, KIR3DX1, LAIR1, LAIR2, LENG8, LENG9, LILRA2, LILRA4, LILRA5, TTYH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599170
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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