A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18151312



Internal ID20718352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103070077..103099733hg38UCSC Ensembl
chr7:102710524..102740180hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3829657
hg1929657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6603130
Supporting Variants
Samples
Known GenesARMC10, FBXL13, NAPEPLD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18151312
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