A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583121



Internal ID20956192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67623607..67624348hg38UCSC Ensembl
chr15:67915945..67916686hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38742
hg19742
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239591
Samples
Known GenesMAP2K5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583121
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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