A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554494



Internal ID20927588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:179143756..179144311hg38UCSC Ensembl
chr1:179112891..179113446hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247823
Samples
Known GenesABL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554494
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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