A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060608



Internal ID19149827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:24693097..24710481hg38UCSC Ensembl
Innerchr16:24704418..24721802hg19UCSC Ensembl
Innerchr16:24611919..24629303hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3817385
hg1917385
hg1817385
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3549128, nssv3549129
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)nsv1060608
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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