A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv624380



Internal ID15847916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:13882281..13883893hg38UCSC Ensembl
Outerchr6:13882512..13884124hg19UCSC Ensembl
Outerchr6:13990491..13992103hg18UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg381613
hg191613
hg181613
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511850
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)nssv624380
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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