A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv547638



Internal ID16335047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:121739361..121743365hg38UCSC Ensembl
Innerchr1:121481159..121485163hg19UCSC Ensembl
Innerchr1:121182682..121186686hg18UCSC Ensembl
Cytoband1p11.1
Allele length
AssemblyAllele length
hg384005
hg194005
hg184005
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv723036
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv547638
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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