A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799831



Internal ID19177827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:58342013..58740459hg38UCSC Ensembl
Innerchr4:59208179..59606624hg19UCSC Ensembl
Innerchr4:58902936..59301381hg18UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38398447
hg19398446
hg18398446
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893924
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=55
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799831
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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