A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2804562



Internal ID21249900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9616901..9618665hg38UCSC Ensembl
chr15:20022212..20024079hg19UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381765
hg191868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13705177
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2804562
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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