A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536469



Internal ID20909816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:61798229..61798888hg38UCSC Ensembl
chr1:62263901..62264560hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38660
hg19660
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250495
Samples
Known GenesINADL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536469
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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