A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844



Internal ID15550694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:93004107..93037135hg38UCSC Ensembl
Outerchr7:92633421..92666449hg19UCSC Ensembl
Outerchr7:92471357..92504385hg18UCSC Ensembl
Outerchr7:92278072..92311100hg17UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg386998
hg196998
hg186998
hg176998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2672
SamplesNA18555
Known Genes
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)nsv5844
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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