A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18151500



Internal ID20718540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157116114..157127752hg38UCSC Ensembl
chr7:156908808..156920446hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3811639
hg1911639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6423929
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18151500
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