A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535773



Internal ID20909126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:58700297..58701442hg38UCSC Ensembl
chr1:59165969..59167114hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg381146
hg191146
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv200n223
Supporting Variantsnssv18250427
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535773
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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