A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611540



Internal ID20984611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98271452..98273171hg38UCSC Ensembl
chr7:97900764..97902483hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg381720
hg191720
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161257
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611540
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