A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576977



Internal ID20950048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:30343797..30489647hg38UCSC Ensembl
chr10:30632726..30778576hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38145851
hg19145851
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233010
Samples
Known GenesMAP3K8, MIR7162, MTPAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576977
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