A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154004



Internal ID20721044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149072532..149075535hg38UCSC Ensembl
chr7:148769624..148772627hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg383004
hg193004
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425334
Supporting Variants
Samples
Known GenesZNF786
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154004
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer