A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17980187



Internal ID20547227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4240601..4251000hg38UCSC Ensembl
chr10:4282793..4293192hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3810400
hg1910400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439871
Supporting Variants
Samples
Known GenesLINC00702
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17980187
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