A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577740



Internal ID20950811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:30678137..30678844hg38UCSC Ensembl
chr12:30831071..30831778hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38708
hg19708
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233453
Samples
Known GenesIPO8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577740
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