A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9039



Internal ID15534825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:65515290..65542951hg38UCSC Ensembl
Outerchr12:65909070..65936731hg19UCSC Ensembl
Outerchr12:64195337..64222998hg18UCSC Ensembl
Outerchr12:64195337..64222998hg17UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg3827662
hg1927662
hg1827662
hg1727662
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv753
Supporting Variants
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)nssv9039
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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