A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559790



Internal ID18858071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:80616871..80641945hg38UCSC Ensembl
Innerchr16:80650768..80675842hg19UCSC Ensembl
Innerchr16:79208269..79233343hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3825075
hg1925075
hg1825075
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057562
Supporting Variants
Samples
Known GenesCDYL2, MIR548H4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559790
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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