A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105600



Internal ID22014833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54297005..54577177hg38UCSC Ensembl
chr19:54807621..55088644hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38280173
hg19281024
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17618301
Samples
Known GenesCDC42EP5, KIR3DX1, LAIR1, LAIR2, LENG8, LENG9, LILRA2, LILRA4, LILRA5, TTYH1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105600
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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