A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545362



Internal ID16332771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:9317805..9353587hg38UCSC Ensembl
Innerchr1:9377864..9413646hg19UCSC Ensembl
Innerchr1:9300451..9336233hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3835783
hg1935783
hg1835783
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1173664
Samples1780854065_A
Known GenesSPSB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545362
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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