A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605357



Internal ID20978428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27981479..27982058hg38UCSC Ensembl
chr7:28021098..28021677hg19UCSC Ensembl
Cytoband7p15.1
Allele length
AssemblyAllele length
hg38580
hg19580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18157057
Samples
Known GenesJAZF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605357
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