A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2805073



Internal ID21250411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:49856634..49856729hg38UCSC Ensembl
chr22:50250282..50250377hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13705179
Samples
Known GenesZBED4
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2805073
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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