A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6479



Internal ID15537384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:103774109..103805788hg38UCSC Ensembl
Outerchr11:103644837..103676516hg19UCSC Ensembl
Outerchr11:103150047..103181726hg18UCSC Ensembl
Outerchr11:103150047..103181726hg17UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg387746
hg197746
hg187746
hg177746
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv467
Supporting Variants
SamplesNA12156
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)nssv6479
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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