A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6427



Internal ID15190751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:132350935..132365269hg38UCSC Ensembl
Outerchr10:134164439..134178773hg19UCSC Ensembl
Outerchr10:134014429..134028763hg18UCSC Ensembl
Outerchr10:134014429..134028763hg17UCSC 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 StatusS
Merged Variantsnsv7627
Supporting Variants
SamplesNA12156
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)nssv6427
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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