A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547608



Internal ID20920809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:62139262..62139825hg38UCSC Ensembl
chr1:62604934..62605497hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38564
hg19564
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250529
Samples
Known GenesINADL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547608
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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