A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545528



Internal ID16332937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:12857981..13050003hg38UCSC Ensembl
Innerchr1:12917836..13052921hg19UCSC Ensembl
Innerchr1:12840423..12975508hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38192023
hg19135086
hg18135086
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv134n54
Supporting Variantsnssv710203
Samples
Known GenesPRAMEF10, PRAMEF2, PRAMEF22, PRAMEF4, PRAMEF6, PRAMEF7, PRAMEF8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545528
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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