A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3755



Internal ID15191797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:133306965..133316658hg38UCSC Ensembl
Outerchr9:136182361..136183495hg19UCSC Ensembl
Outerchr9:135172182..135173316hg18UCSC Ensembl
Outerchr9:133211915..133213049hg17UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg388273
hg198273
hg188273
hg178273
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6749
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)nssv3755
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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