A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601770



Internal ID20974841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:88433331..88433866hg38UCSC Ensembl
chr7:88062646..88063181hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161952
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601770
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