A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4586



Internal ID15549310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:163567744..163603252hg38UCSC Ensembl
Outerchr4:164488896..164524404hg19UCSC Ensembl
Outerchr4:164708346..164743854hg18UCSC Ensembl
Outerchr4:164846501..164882009hg17UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg384239
hg194239
hg184239
hg174239
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3299
SamplesNA12878
Known GenesMARCH1
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)nsv4586
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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