A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4552



Internal ID15549273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:151760059..151781305hg38UCSC Ensembl
Outerchr4:152681211..152702457hg19UCSC Ensembl
Outerchr4:152900661..152921907hg18UCSC Ensembl
Outerchr4:153038816..153060062hg17UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3821247
hg1921247
hg1821247
hg1721247
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8013
SamplesNA12156
Known GenesPET112
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)nsv4552
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