A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv624698



Internal ID15501548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1540441..1542123hg38UCSC Ensembl
Outerchr10:1582636..1584318hg19UCSC Ensembl
Outerchr10:1572636..1574318hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg381683
hg191683
hg181683
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512138
Supporting Variants
Samples1
Known GenesADARB2, ADARB2-AS1
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv624698
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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