A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1777



Internal ID15199654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:86837468..86872105hg38UCSC Ensembl
Outerchr1:87303151..87337788hg19UCSC Ensembl
Outerchr1:87075739..87110376hg18UCSC Ensembl
Outerchr1:87015172..87049809hg17UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg385391
hg195391
hg185391
hg175391
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2994
SamplesNA18555
Known GenesSEP15
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)nsv1777
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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