A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427801



Internal ID21085354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139441369..139442922hg38UCSC Ensembl
chr7:139126115..139127668hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381554
hg191554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155256
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427801
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