A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061200



Internal ID19150419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:63488443..63691706hg38UCSC Ensembl
Innerchr16:63522347..63725610hg19UCSC Ensembl
Innerchr16:62079848..62283111hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38203264
hg19203264
hg18203264
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559387
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)nsv1061200
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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