A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420162



Internal ID21077715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:134446601..134477500hg38UCSC Ensembl
chr7:134131353..134162252hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3830900
hg1930900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151712
Samples
Known GenesAKR1B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420162
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