A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552336



Internal ID20925463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:59506535..59507527hg38UCSC Ensembl
chr1:59972207..59973199hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38993
hg19993
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv202n223
Supporting Variantsnssv18250435
Samples
Known GenesFGGY
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552336
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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