A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605860



Internal ID20978931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:86807001..86807300hg38UCSC Ensembl
chr7:86436317..86436616hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18160437
Samples
Known GenesGRM3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605860
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