A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585972



Internal ID20959043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78898516..78899348hg38UCSC Ensembl
chr15:79190858..79191690hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38833
hg19833
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239738
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585972
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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