A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9936



Internal ID15193338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:132351135..132375206hg38UCSC Ensembl
Outerchr10:134164639..134188710hg19UCSC Ensembl
Outerchr10:134014629..134038700hg18UCSC Ensembl
Outerchr10:134014629..134038700hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg389289
hg199289
hg189289
hg179289
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7627
Supporting Variants
SamplesNA18507
Known GenesLRRC27
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)nssv9936
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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