A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539180



Internal ID20859636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173428059..173428712hg38UCSC Ensembl
chr1:173397198..173397851hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg38654
hg19654
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248108
Samples
Known GenesLOC100506023
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539180
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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