A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800624



Internal ID19175701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:148712561..148739759hg38UCSC Ensembl
Innerchr4:149633713..149660911hg19UCSC Ensembl
Innerchr4:149853163..149880361hg18UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg3827199
hg1927199
hg1827199
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894051
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800624
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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