A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594553



Internal ID20967624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34030075..34030459hg38UCSC Ensembl
chr15:34322276..34322660hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38385
hg19385
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239528
Samples
Known GenesAVEN, CHRM5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594553
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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