A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2795935



Internal ID21241274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58710653..58710738hg38UCSC Ensembl
chr16:58744557..58744642hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13687607
Samples
Known GenesGOT2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2795935
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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