A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581296



Internal ID20954367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31108597..31109343hg38UCSC Ensembl
chr15:31400800..31401546hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38747
hg19747
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239487
Samples
Known GenesTRPM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581296
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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