A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2804117



Internal ID21249455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44733300..44733364hg38UCSC Ensembl
chr21:46153215..46153279hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13689515
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2804117
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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