A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2808733



Internal ID21254071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:63270858..63270964hg38UCSC Ensembl
chr3:63256534..63256640hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13677714
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2808733
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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