A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1702



Internal ID15546265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:751088..784288hg38UCSC Ensembl
Outerchr16:801088..834288hg19UCSC Ensembl
Outerchr16:741089..774289hg18UCSC Ensembl
Outerchr16:741089..774289hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg387784
hg197784
hg187784
hg177784
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1285
SamplesNA19240
Known GenesMIR662, MSLN
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)nsv1702
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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