A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545587



Internal ID16332996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:14350414..14377358hg38UCSC Ensembl
Innerchr1:14676909..14703854hg19UCSC Ensembl
Innerchr1:14549496..14576441hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3826945
hg1926946
hg1826946
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1173769
Samples1780862466_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545587
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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