A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587952



Internal ID20961023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:96231631..96232243hg38UCSC Ensembl
chr12:96625409..96626021hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38613
hg19613
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235839
Samples
Known GenesELK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587952
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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