A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4567



Internal ID15549289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:156201407..156234667hg38UCSC Ensembl
Outerchr4:157122559..157155819hg19UCSC Ensembl
Outerchr4:157342009..157375269hg18UCSC Ensembl
Outerchr4:157480164..157513424hg17UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg386024
hg196024
hg186024
hg176024
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4792
SamplesNA19129
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)nsv4567
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