A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5372n100



Internal ID20156988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:118028335..118350088hg38UCSC Ensembl
chr4:118949490..119271243hg19UCSC Ensembl
chr4:119168938..119490691hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38321754
hg19321754
hg18321754
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1001236, nsv1009076
Samples
Known GenesNDST3, PRSS12, SNHG8, SNORA24
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5372n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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