A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542624



Internal ID20915882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:85210264..85215743hg38UCSC Ensembl
chr2:85437387..85442866hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg385480
hg195480
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260901
Samples
Known GenesTCF7L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542624
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