A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv624436



Internal ID15847972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:77716676..77726379hg38UCSC Ensembl
Outerchr6:78426393..78436096hg19UCSC Ensembl
Outerchr6:78483112..78492815hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg389704
hg199704
hg189704
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511901
Supporting Variants
Samples1
Known GenesMEI4
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv624436
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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