A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18152660



Internal ID20719700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12711121..12737124hg38UCSC Ensembl
chr7:12750746..12776749hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3826004
hg1926004
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617103
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18152660
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