A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580652



Internal ID20953723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:106725618..106726574hg38UCSC Ensembl
chr12:107119396..107120352hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38957
hg19957
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229133
Samples
Known GenesLOC100287944, RFX4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580652
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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