A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177376



Internal ID20744416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50412901..50420100hg38UCSC Ensembl
chr10:52172661..52179860hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg387200
hg197200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452286
Supporting Variants
Samples
Known GenesSGMS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177376
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00018


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