A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545678



Internal ID15986401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16906708..16921023hg38UCSC Ensembl
Innerchr1:17233203..17247518hg19UCSC Ensembl
Innerchr1:17105790..17120105hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3814316
hg1914316
hg1814316
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv710906, nssv710904, nssv710905, nssv710903
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545678
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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