A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5164



Internal ID15549946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:311655..332372hg38UCSC Ensembl
Outerchr6:311655..332372hg19UCSC Ensembl
Outerchr6:256655..277372hg18UCSC Ensembl
Outerchr6:256655..277372hg17UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg386691
hg196691
hg186691
hg176691
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2717
SamplesNA18555
Known GenesDUSP22
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)nsv5164
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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