A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856



Internal ID15550707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:96012519..96047730hg38UCSC Ensembl
Outerchr7:95641831..95677042hg19UCSC Ensembl
Outerchr7:95479767..95514978hg18UCSC Ensembl
Outerchr7:95286482..95321693hg17UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg385775
hg195775
hg185775
hg175775
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv659
SamplesNA19240
Known GenesDYNC1I1
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)nsv5856
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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