A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537485



Internal ID20910819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:234470040..234470596hg38UCSC Ensembl
chr1:234605786..234606342hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg38557
hg19557
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250671
Samples
Known GenesTARBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537485
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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