A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062724



Internal ID18805255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:81018707..81103402hg38UCSC Ensembl
Innerchr16:81052312..81137007hg19UCSC Ensembl
Innerchr16:79609813..79694508hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3884696
hg1984696
hg1884696
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559815
Samples
Known GenesATMIN, C16orf46, CENPN, GCSH, PKD1L2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062724
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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