A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419801



Internal ID21077354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141841078..141841512hg38UCSC Ensembl
chr7:141540878..141541312hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38435
hg19435
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150783
Samples
Known GenesPRSS37
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419801
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