A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv624963



Internal ID15848499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:102170617..102173506hg38UCSC Ensembl
Outerchr14:102636954..102639843hg19UCSC Ensembl
Outerchr14:101706707..101709596hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg382890
hg192890
hg182890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512376
Supporting Variants
Samples1
Known GenesWDR20
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv624963
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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