A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861



Internal ID15550713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:98540420..98549386hg38UCSC Ensembl
Outerchr7:98169732..98178698hg19UCSC Ensembl
Outerchr7:98007668..98016634hg18UCSC Ensembl
Outerchr7:97814383..97823349hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg385457
hg195457
hg185457
hg175457
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8405
SamplesNA12156
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)nsv5861
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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