A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625891



Internal ID15849424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:78350475..78351579hg38UCSC Ensembl
Outerchr17:76346556..76347660hg19UCSC Ensembl
Outerchr17:73858151..73859255hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38797
hg19797
hg18797
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513484
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)nssv625891
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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