A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1004277



Internal ID16298233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:109919592..109921720hg38UCSC Ensembl
Innerchr4:110840748..110842876hg19UCSC Ensembl
Innerchr4:111060197..111062325hg18UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg382129
hg192129
hg182129
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595143
Supporting Variants
Samples
Known GenesEGF
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1004277
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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