A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892761



Internal ID22667816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63784658..63787190hg38UCSC Ensembl
chr6:64494551..64497083hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg382533
hg192533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444508
Samples
Known GenesEYS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892761
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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