A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577042



Internal ID20950113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25752491..25753492hg38UCSC Ensembl
chr15:25997638..25998639hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg381002
hg191002
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2467n223
Supporting Variantsnssv18239400
Samples
Known GenesATP10A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577042
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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