A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv624736



Internal ID15848272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:81369894..81371429hg38UCSC Ensembl
Outerchr10:83129650..83131185hg19UCSC Ensembl
Outerchr10:83119630..83121165hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg381536
hg191536
hg181536
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512171
Supporting Variants
Samples1
Known Genes
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv624736
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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