A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2804344



Internal ID21249682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:12698690..12699025hg38UCSC Ensembl
chrUn_gl000235:6960..7295hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13699265
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2804344
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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