A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891857



Internal ID18839567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:72086126..72148450hg38UCSC Ensembl
Outerchr10:72086126..72148450hg38UCSC Ensembl
Innerchr10:73845884..73908208hg19UCSC Ensembl
Outerchr10:73845884..73908208hg19UCSC Ensembl
Innerchr10:73515890..73578214hg18UCSC Ensembl
Outerchr10:73515890..73578214hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3862325
hg1962325
hg1862325
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25778646
Samples
Known GenesASCC1, SPOCK2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891857
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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