A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790556



Internal ID19171929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:64610069..65067872hg38UCSC Ensembl
Innerchr10:66369826..66827630hg19UCSC Ensembl
Innerchr10:66039832..66497636hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38457804
hg19457805
hg18457805
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891832
Supporting Variants
Samples
Known GenesANXA2P3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=100
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790556
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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