A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4277



Internal ID15202284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:25127698..25172730hg38UCSC Ensembl
Outerchr4:25129320..25174352hg19UCSC Ensembl
Outerchr4:24738418..24783450hg18UCSC Ensembl
Outerchr4:24805589..24850621hg17UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3845033
hg1945033
hg1845033
hg1745033
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7939
SamplesNA12156
Known GenesSEPSECS, SEPSECS-AS1
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)nsv4277
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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