A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9955



Internal ID15193361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:102684331..102714277hg38UCSC Ensembl
Outerchr13:103336681..103366627hg19UCSC Ensembl
Outerchr13:102134682..102164628hg18UCSC Ensembl
Outerchr13:102134682..102164628hg17UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg386126
hg196126
hg186126
hg176126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1157
Supporting Variants
SamplesNA18507
Known GenesMETTL21C
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)nssv9955
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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