A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577153



Internal ID20950224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122342791..122342882hg38UCSC Ensembl
chr12:122827338..122827429hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235714
Samples
Known GenesCLIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577153
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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