A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5727



Internal ID15550565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:47055682..47085070hg38UCSC Ensembl
Outerchr7:47095280..47124668hg19UCSC Ensembl
Outerchr7:47061805..47091193hg18UCSC Ensembl
Outerchr7:46868520..46897908hg17UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3829389
hg1929389
hg1829389
hg1729389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4977, nssv8370
SamplesNA12156, NA19129
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)nsv5727
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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