A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041551



Internal ID19130770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7983841..8006576hg38UCSC Ensembl
Innerchr16:8033843..8056578hg19UCSC Ensembl
Innerchr16:7973844..7996579hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3822736
hg1922736
hg1822736
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2722n100
Supporting Variantsnssv3718867
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)nsv1041551
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