A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539258



Internal ID20912559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:59506526..59507512hg38UCSC Ensembl
chr1:59972198..59973184hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38987
hg19987
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv202n223
Supporting Variantsnssv18250434
Samples
Known GenesFGGY
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539258
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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