A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800378



Internal ID19180102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:114968082..115003389hg38UCSC Ensembl
Innerchr4:115889238..115924545hg19UCSC Ensembl
Innerchr4:116108687..116143994hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3835308
hg1935308
hg1835308
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894008
Supporting Variants
Samples
Known GenesNDST4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800378
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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