A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582846



Internal ID20955917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44983367..44983584hg38UCSC Ensembl
chr13:45557502..45557719hg19UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg38218
hg19218
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1816n223
Supporting Variantsnssv18226703
Samples
Known GenesNUFIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582846
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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