A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558



Internal ID15550379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:157916017..157960776hg38UCSC Ensembl
Outerchr6:158337049..158381808hg19UCSC Ensembl
Outerchr6:158257037..158301796hg18UCSC Ensembl
Outerchr6:158307458..158352217hg17UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3844760
hg1944760
hg1844760
hg1744760
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4951
SamplesNA19129
Known GenesSNX9
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)nsv5558
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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