A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5678



Internal ID15203825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:28280351..28325206hg38UCSC Ensembl
Outerchr7:28319970..28364825hg19UCSC Ensembl
Outerchr7:28286495..28331350hg18UCSC Ensembl
Outerchr7:28093210..28138065hg17UCSC Ensembl
Cytoband7p15.1
Allele length
AssemblyAllele length
hg3844856
hg1944856
hg1844856
hg1744856
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8352
SamplesNA12156
Known GenesCREB5
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)nsv5678
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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