A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582292



Internal ID20955363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:62393999..62394544hg38UCSC Ensembl
chr12:62787779..62788324hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg38546
hg19546
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232437
Samples
Known GenesUSP15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582292
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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