A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25778646



Internal ID18828966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:72086126..72148450hg38UCSC Ensembl
Innerchr10:73845884..73908208hg19UCSC Ensembl
Innerchr10:73515890..73578214hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3862325
hg1962325
hg1862325
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891857
Supporting Variants
Samples
Known GenesASCC1, SPOCK2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25778646
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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