A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580224



Internal ID20953295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:51073630..51074261hg38UCSC Ensembl
chr12:51467413..51468044hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg38632
hg19632
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226908
Samples
Known GenesCSRNP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580224
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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