A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2809846



Internal ID21255184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:182815221..182815403hg38UCSC Ensembl
chr4:183736374..183736556hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13687377
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2809846
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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