A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2795183



Internal ID21240521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56397704..56397967hg38UCSC Ensembl
chr16:56431616..56431879hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv112n137
Supporting Variantsnssv13684174
Samples
Known GenesAMFR
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2795183
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer