A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7627



Internal ID15205969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:132350184..132375206hg38UCSC Ensembl
Outerchr10:134163688..134188710hg19UCSC Ensembl
Outerchr10:134013678..134038700hg18UCSC Ensembl
Outerchr10:134013678..134038700hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3810124
hg1910124
hg1810124
hg1710124
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9936, nssv6427, nssv3910
SamplesNA18507, NA12156, NA12878
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)nsv7627
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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