A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559422



Internal ID18857703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:64044716..64080299hg38UCSC Ensembl
Innerchr16:64078620..64114203hg19UCSC Ensembl
Innerchr16:62636121..62671704hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3835584
hg1935584
hg1835584
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062072
Supporting Variants
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)nssv3559422
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