A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv972945



Internal ID15920215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:127628987..127638952hg38UCSC Ensembl
Innerchr3:127347830..127357795hg19UCSC Ensembl
Innerchr3:128830520..128840485hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg389966
hg199966
hg189966
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591584
Supporting Variants
Samples
Known GenesPODXL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv972945
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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