A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv668



Internal ID15551613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:33128741..33161949hg38UCSC Ensembl
Outerchr12:33281675..33314883hg19UCSC Ensembl
Outerchr12:33172942..33206150hg18UCSC Ensembl
Outerchr12:33172942..33206150hg17UCSC Ensembl
Cytoband12p11.1
Allele length
AssemblyAllele length
hg3833209
hg1933209
hg1833209
hg1733209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9834
SamplesNA18507
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)nsv668
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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