A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4184



Internal ID15192225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:841017..861812hg38UCSC Ensembl
Outerchr16:891017..911812hg19UCSC Ensembl
Outerchr16:831018..851813hg18UCSC Ensembl
Outerchr16:831018..851813hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg385213
hg195213
hg185213
hg175213
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1704
Supporting Variants
SamplesNA12878
Known GenesLMF1
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)nssv4184
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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