A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549874



Internal ID20923024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61128521..61129314hg38UCSC Ensembl
chr2:61355656..61356449hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38794
hg19794
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257696
Samples
Known GenesKIAA1841
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549874
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