A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546554



Internal ID20876240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35333274..35334319hg38UCSC Ensembl
chr1:35798875..35799920hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381046
hg191046
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250392
Samples
Known GenesZMYM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546554
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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