A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9232n54



Internal ID22777127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:115007591..115008123hg38UCSC Ensembl
chr4:115928747..115929279hg19UCSC Ensembl
chr4:116148196..116148728hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38533
hg19533
hg18533
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv595229, nsv595233
Samples
Known GenesNDST4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9232n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss203
Observed Complex0
Frequencyn/a


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