A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7622



Internal ID15552650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:131271324..131286917hg38UCSC Ensembl
Outerchr10:133069587..133085180hg19UCSC Ensembl
Outerchr10:132959577..132975170hg18UCSC Ensembl
Outerchr10:132959577..132975170hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg386264
hg196264
hg186264
hg176264
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv974
SamplesNA19240
Known GenesTCERG1L
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)nsv7622
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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