A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545171



Internal ID16332580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:5693290..5827080hg38UCSC Ensembl
Innerchr1:5753350..5887140hg19UCSC Ensembl
Innerchr1:5675937..5809727hg18UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg38133791
hg19133791
hg18133791
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv708950
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545171
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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