A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661



Internal ID15203807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:23265261..23296177hg38UCSC Ensembl
Outerchr7:23304880..23335796hg19UCSC Ensembl
Outerchr7:23271405..23302321hg18UCSC Ensembl
Outerchr7:23078120..23109036hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg388460
hg198460
hg188460
hg178460
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10538
SamplesNA18956
Known GenesGPNMB
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)nsv5661
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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