A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545412



Internal ID16332821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:11433775..11460596hg38UCSC Ensembl
Innerchr1:11493832..11520653hg19UCSC Ensembl
Innerchr1:11416419..11443240hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3826822
hg1926822
hg1826822
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1173671
Samples1780854097_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545412
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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