A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784719



Internal ID19172167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:14879753..15249761hg38UCSC Ensembl
Innerchr8:14737262..15107270hg19UCSC Ensembl
Innerchr8:14781633..15151641hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38370009
hg19370009
hg18370009
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891347
Supporting Variants
Samples
Known GenesSGCZ
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=321
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784719
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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