A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370976



Internal ID21028529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:112044359..112045186hg38UCSC Ensembl
chr3:111763206..111764033hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg38828
hg19828
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092115
Samples
Known GenesTMPRSS7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370976
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer