A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10413



Internal ID15542385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:90661242..90691819hg38UCSC Ensembl
Outerchr4:91582393..91612970hg19UCSC Ensembl
Outerchr4:91801416..91831993hg18UCSC Ensembl
Outerchr4:91939571..91970148hg17UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3830578
hg1930578
hg1830578
hg1730578
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4419
Supporting Variants
SamplesNA18956
Known GenesCCSER1
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)nssv10413
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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