A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057968



Internal ID19147187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:64122308..64197360hg38UCSC Ensembl
Innerchr16:64156212..64231264hg19UCSC Ensembl
Innerchr16:62713713..62788765hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3875053
hg1975053
hg1875053
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559430
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)nsv1057968
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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