A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1894



Internal ID15546457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:79759889..79790591hg38UCSC Ensembl
Outerchr16:79793786..79824488hg19UCSC Ensembl
Outerchr16:78351287..78381989hg18UCSC Ensembl
Outerchr16:78351287..78381989hg17UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg388555
hg198555
hg188555
hg178555
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5618
SamplesNA19129
Known GenesLOC101928248, LOC102467146
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)nsv1894
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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