A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7738



Internal ID15552777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:38106005..38142277hg38UCSC Ensembl
Outerchr11:38127555..38163827hg19UCSC Ensembl
Outerchr11:38084131..38120403hg18UCSC Ensembl
Outerchr11:38084131..38120403hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3836273
hg1936273
hg1836273
hg1736273
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8898
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)nsv7738
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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