A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625886



Internal ID15502733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:73405128..73405248hg38UCSC Ensembl
Outerchr17:71401267..71401387hg19UCSC Ensembl
Outerchr17:68912862..68912982hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg381174
hg191174
hg181174
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513480
Supporting Variants
Samples1
Known GenesSDK2
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv625886
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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