A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4419



Internal ID15549126
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 Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4765, nssv3271, nssv10413, nssv2474, nssv7105
SamplesNA12156, NA12878, NA18956, NA18555, NA19129
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)nsv4419
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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