A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603458



Internal ID20976529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:116894901..116895800hg38UCSC Ensembl
chr7:116534955..116535854hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18148603
Samples
Known GenesCAPZA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603458
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