A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv544873



Internal ID16332282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:121042..170730hg38UCSC Ensembl
Innerchr1:121042..170730hg19UCSC Ensembl
Innerchr1:110905..160593hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3849689
hg1949689
hg1849689
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv707623
Samples
Known GenesLOC729737
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv544873
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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