A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2817852



Internal ID21263190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:38241961..38242040hg38UCSC Ensembl
chr9:38241958..38242037hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13706680
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2817852
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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