A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453903



Internal ID21111456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118007835..118008689hg38UCSC Ensembl
chr10:119767346..119768200hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38855
hg19855
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978343
Samples
Known GenesRAB11FIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453903
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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