A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3395



Internal ID15538123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:154316156..154348055hg38UCSC Ensembl
Outerchr5:153695716..153727615hg19UCSC Ensembl
Outerchr5:153675909..153707808hg18UCSC Ensembl
Outerchr5:153675909..153707808hg17UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg387827
hg197827
hg187827
hg177827
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5079
Supporting Variants
SamplesNA12878
Known GenesGALNT10
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)nssv3395
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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