A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv624987



Internal ID15848523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:64338257..64341813hg38UCSC Ensembl
Outerchr15:64630456..64634012hg19UCSC Ensembl
Outerchr15:62417509..62421065hg18UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg383557
hg193557
hg183557
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512398
Supporting Variants
Samples1
Known GenesCSNK1G1
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv624987
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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