A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545468



Internal ID15986191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:12800601..12851347hg38UCSC Ensembl
Innerchr1:12860749..12911200hg19UCSC Ensembl
Innerchr1:12783336..12833787hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3850747
hg1950452
hg1850452
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv124n54
Supporting Variantsnssv1173688, nssv1173689
SamplesHGDP01296, HGDP00791
Known GenesHNRNPCL1, LOC649330, PRAMEF11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545468
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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