A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592234



Internal ID20965305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64431902..64432513hg38UCSC Ensembl
chr15:64724101..64724712hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38612
hg19612
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238831
Samples
Known GenesTRIP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592234
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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