A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626307



Internal ID15503154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:933871..935480hg38UCSC Ensembl
Outerchr1:869251..870860hg19UCSC Ensembl
Outerchr1:859114..860723hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg381610
hg191610
hg181610
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511670
Supporting Variants
Samples1
Known GenesSAMD11
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626307
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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