A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5192



Internal ID15549977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:8318727..8373649hg38UCSC Ensembl
Outerchr6:8318960..8373882hg19UCSC Ensembl
Outerchr6:8263959..8318881hg18UCSC Ensembl
Outerchr6:8263959..8318881hg17UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3854923
hg1954923
hg1854923
hg1754923
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8219, nssv8218
SamplesNA12156
Known Genes
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)nsv5192
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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