A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1923



Internal ID15194520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:3238060..3296031hg38UCSC Ensembl
Outerchr11:3259290..3317261hg19UCSC Ensembl
Outerchr11:3215866..3273837hg18UCSC Ensembl
Outerchr11:3215866..3273837hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3857972
hg1957972
hg1857972
hg1757972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7649
Supporting Variants
SamplesNA18555
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)nssv1923
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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