A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626331



Internal ID15849864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:56365410..56369557hg38UCSC Ensembl
Outerchr1:56831082..56835229hg19UCSC Ensembl
Outerchr1:56603670..56607817hg18UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg384148
hg194148
hg184148
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511692
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)nssv626331
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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