A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv624757



Internal ID15848293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:126056394..126057527hg38UCSC Ensembl
Outerchr10:127744963..127746096hg19UCSC Ensembl
Outerchr10:127734953..127736086hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg381134
hg191134
hg181134
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512190
Supporting Variants
Samples1
Known GenesADAM12
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv624757
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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