A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4571



Internal ID15549294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:158944764..158989467hg38UCSC Ensembl
Outerchr4:159865916..159910619hg19UCSC Ensembl
Outerchr4:160085366..160130069hg18UCSC Ensembl
Outerchr4:160223521..160268224hg17UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3844704
hg1944704
hg1844704
hg1744704
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8018
SamplesNA12156
Known GenesC4orf45
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)nsv4571
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