A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551284



Internal ID20924421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61547605..61547952hg38UCSC Ensembl
chr2:61774740..61775087hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258321
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551284
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