A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17978344



Internal ID20545384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118011201..118012800hg38UCSC Ensembl
chr10:119770712..119772311hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442120
Supporting Variants
Samples
Known GenesRAB11FIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17978344
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00065


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