A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545092



Internal ID16332501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:2683129..2701859hg38UCSC Ensembl
Innerchr1:2614568..2633298hg19UCSC Ensembl
Innerchr1:2604428..2623158hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3818731
hg1918731
hg1818731
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv708760
Samples
Known GenesTTC34
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545092
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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