A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9078



Internal ID15534786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:108573153..108587634hg38UCSC Ensembl
Outerchr12:108966929..108981410hg19UCSC Ensembl
Outerchr12:107491058..107505539hg18UCSC Ensembl
Outerchr12:107469395..107483876hg17UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg386138
hg196138
hg186138
hg176138
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv882
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)nssv9078
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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