A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537914



Internal ID20911243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157742144..157743963hg38UCSC Ensembl
chr1:157711934..157713753hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg381820
hg191820
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247768
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537914
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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