A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428362



Internal ID21085915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128495107..128499732hg38UCSC Ensembl
chr7:128135161..128139786hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg384626
hg194626
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153308
Samples
Known GenesMETTL2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428362
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