A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155528



Internal ID20722568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25310826..25333993hg38UCSC Ensembl
chr7:25350445..25373612hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3823168
hg1923168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610456
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155528
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