A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354868



Internal ID21012421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:226903574..226990920hg38UCSC Ensembl
chr2:227768290..227855636hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg3887347
hg1987347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18087033
Samples
Known GenesRHBDD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354868
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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