A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10031



Internal ID15542766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:94450081..94477913hg38UCSC Ensembl
Outerchr14:94916418..94944250hg19UCSC Ensembl
Outerchr14:93986171..94014003hg18UCSC Ensembl
Outerchr14:93986171..94014003hg17UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg386708
hg196708
hg186708
hg176708
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1407
Supporting Variants
SamplesNA18956
Known GenesSERPINA11, SERPINA9
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv10031
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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