A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv438



Internal ID15202397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:93301245..93347347hg38UCSC Ensembl
Outerchr11:93034411..93080513hg19UCSC Ensembl
Outerchr11:92674059..92720161hg18UCSC Ensembl
Outerchr11:92674059..92720161hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3846103
hg1946103
hg1846103
hg1746103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6475
SamplesNA12156
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)nsv438
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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