A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2808606



Internal ID21253944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184624467..184624586hg38UCSC Ensembl
chr4:185545621..185545740hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13679413
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2808606
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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