A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576198



Internal ID20949269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8640763..8641724hg38UCSC Ensembl
chr12:8793359..8794320hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38962
hg19962
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221070
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576198
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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