A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612797



Internal ID20985868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:111810342..111810901hg38UCSC Ensembl
chr7:111450398..111450957hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149522
Samples
Known GenesDOCK4, DOCK4-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612797
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