A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2804463



Internal ID21249801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39357601..39357662hg38UCSC Ensembl
chr22:39753606..39753667hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13699437
Samples
Known GenesSYNGR1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2804463
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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