A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419761



Internal ID21077314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:144842465..144847781hg38UCSC Ensembl
chr7:144539558..144544874hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg385317
hg195317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153153
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419761
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