A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626515



Internal ID15850048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:8410580..8413558hg38UCSC Ensembl
Outerchr3:8452266..8455244hg19UCSC Ensembl
Outerchr3:8427266..8430244hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg382979
hg192979
hg182979
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513033
Supporting Variants
Samples1
Known GenesLMCD1-AS1
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626515
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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