A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11152



Internal ID15539427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:95953923..95981823hg38UCSC Ensembl
Outerchr7:95583235..95611135hg19UCSC Ensembl
Outerchr7:95421171..95449071hg18UCSC Ensembl
Outerchr7:95227886..95255786hg17UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3811972
hg1911972
hg1811972
hg1711972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852
Supporting Variants
SamplesNA15510
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)nssv11152
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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