A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545800



Internal ID20919026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:73845634..73846362hg38UCSC Ensembl
chr2:74072761..74073489hg19UCSC Ensembl
Cytoband2p13.1
Allele length
AssemblyAllele length
hg38729
hg19729
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259010
Samples
Known GenesSTAMBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545800
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer