A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1908



Internal ID15199785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:83876721..83909333hg38UCSC Ensembl
Outerchr16:83910326..83942938hg19UCSC Ensembl
Outerchr16:82467827..82500439hg18UCSC Ensembl
Outerchr16:82467827..82500439hg17UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg387121
hg197121
hg187121
hg177121
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4234
SamplesNA12878
Known GenesMLYCD
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)nsv1908
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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