A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785842



Internal ID19164515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:31452344..31469074hg38UCSC Ensembl
Innerchr10:31741273..31758003hg19UCSC Ensembl
Innerchr10:31781279..31798009hg18UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3816731
hg1916731
hg1816731
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891781
Supporting Variants
Samples
Known GenesZEB1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785842
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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