A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542595



Internal ID20915853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206298707..206299608hg38UCSC Ensembl
chr2:207163431..207164332hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258528
Samples
Known GenesZDBF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542595
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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