A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575004



Internal ID20948075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150730742..150732615hg38UCSC Ensembl
chr3:150448529..150450402hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg381874
hg191874
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263206
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575004
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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