A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591693



Internal ID20964764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36650475..36651000hg38UCSC Ensembl
chr15:36942676..36943201hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38526
hg19526
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237978
Samples
Known GenesC15orf41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591693
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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