A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798468



Internal ID18828248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45884734..45910910hg38UCSC Ensembl
Innerchr10:51684916..51711092hg19UCSC Ensembl
Innerchr10:51354922..51381098hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3826177
hg1926177
hg1826177
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891807
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=9
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798468
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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