A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18153187



Internal ID20720227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:145179781..145180334hg38UCSC Ensembl
chr7:144876874..144877427hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38554
hg19554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426360
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18153187
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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