A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042645



Internal ID19131864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:5697274..5744316hg38UCSC Ensembl
Innerchr16:5747275..5794317hg19UCSC Ensembl
Innerchr16:5687276..5734318hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3847043
hg1947043
hg1847043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2702n100
Supporting Variantsnssv3557010
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042645
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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