A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455289



Internal ID21112842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119314166..119319742hg38UCSC Ensembl
chr10:121073678..121079254hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg385577
hg195577
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979609
Samples
Known GenesGRK5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455289
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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