A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv826



Internal ID15206161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:93729104..93774535hg38UCSC Ensembl
Outerchr12:94122880..94168311hg19UCSC Ensembl
Outerchr12:92647011..92692442hg18UCSC Ensembl
Outerchr12:92625348..92670779hg17UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg3845432
hg1945432
hg1845432
hg1745432
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6527
SamplesNA12156
Known GenesCRADD
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)nsv826
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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