A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7568



Internal ID15205904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:28381292..28412121hg38UCSC Ensembl
Outerchr1:28707803..28738632hg19UCSC Ensembl
Outerchr1:28580390..28611219hg18UCSC Ensembl
Outerchr1:28391945..28422774hg17UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg389198
hg199198
hg189198
hg179198
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2004
SamplesNA18555
Known GenesPHACTR4
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)nsv7568
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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