A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4084



Internal ID15538811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:98579408..98612499hg38UCSC Ensembl
Outerchr13:99231662..99264753hg19UCSC Ensembl
Outerchr13:98029663..98062754hg18UCSC Ensembl
Outerchr13:98029663..98062754hg17UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3833092
hg1933092
hg1833092
hg1733092
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1144
Supporting Variants
SamplesNA12878
Known Genes
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)nssv4084
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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