A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545079



Internal ID16332488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:2459149..2518955hg38UCSC Ensembl
Innerchr1:2390588..2450394hg19UCSC Ensembl
Innerchr1:2380448..2440254hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3859807
hg1959807
hg1859807
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv708748
Samples
Known GenesPANK4, PLCH2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545079
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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