A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3062n100



Internal ID20154678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87725235..87842257hg38UCSC Ensembl
chr16:87758841..87875863hg19UCSC Ensembl
chr16:86316342..86433364hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38117023
hg19117023
hg18117023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1055626, nsv1065400
Samples
Known GenesKLHDC4, MIR6775, SLC7A5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3062n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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