A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154085



Internal ID20721125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131275673..131278806hg38UCSC Ensembl
chr7:130960432..130963565hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg383134
hg193134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6415916
Supporting Variants
Samples
Known GenesMKLN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154085
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