A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915



Internal ID15204086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:116277964..116312979hg38UCSC Ensembl
Outerchr7:115918018..115953033hg19UCSC Ensembl
Outerchr7:115705254..115740269hg18UCSC Ensembl
Outerchr7:115511969..115546984hg17UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg3835016
hg1935016
hg1835016
hg1735016
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv11161
SamplesNA15510
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)nsv5915
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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