A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862



Internal ID15550714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:98753303..98795168hg38UCSC Ensembl
Outerchr7:98382615..98392791hg19UCSC Ensembl
Outerchr7:98220551..98230727hg18UCSC Ensembl
Outerchr7:98027266..98037442hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3830878
hg1930878
hg1830878
hg1730878
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557, nssv662, nssv2675
SamplesNA12878, NA18555, NA19240
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)nsv5862
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer