A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610493



Internal ID20983564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:42941740..42942695hg38UCSC Ensembl
chr7:42981339..42982294hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38956
hg19956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154526
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610493
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