A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064541



Internal ID18807072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32016645..32471086hg38UCSC Ensembl
Innerchr16:32027966..32482407hg19UCSC Ensembl
Innerchr16:31935467..32389908hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38454442
hg19454442
hg18454442
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2835n100
Supporting Variantsnssv3716194
Samples
Known GenesHERC2P4, LOC390705, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064541
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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