A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17977265



Internal ID20544306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102510486..102515563hg38UCSC Ensembl
chr10:104270243..104275320hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg385078
hg195078
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450217
Supporting Variants
Samples
Known GenesSUFU
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17977265
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