A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551129



Internal ID20924269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:61363457..61363949hg38UCSC Ensembl
chr1:61829129..61829621hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38493
hg19493
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250465
Samples
Known GenesNFIA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551129
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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