A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv439



Internal ID15549094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:93402770..93438516hg38UCSC Ensembl
Outerchr11:93135936..93171682hg19UCSC Ensembl
Outerchr11:92775584..92811330hg18UCSC Ensembl
Outerchr11:92775584..92811330hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3835747
hg1935747
hg1835747
hg1735747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5373, nssv6476, nssv1029, nssv1952
SamplesNA12156, NA18555, NA19240, NA19129
Known GenesCCDC67
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)nsv439
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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