A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4016



Internal ID15538743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:25986982..26020423hg38UCSC Ensembl
Outerchr1:26313473..26346914hg19UCSC Ensembl
Outerchr1:26186060..26219501hg18UCSC Ensembl
Outerchr1:25997615..26031056hg17UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg386308
hg196308
hg186308
hg176308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7501
Supporting Variants
SamplesNA12878
Known GenesPAFAH2
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)nssv4016
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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