A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586735



Internal ID20959806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:121225422..121226385hg38UCSC Ensembl
chr12:121663225..121664188hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38964
hg19964
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234731
Samples
Known GenesP2RX4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586735
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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