A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829



Internal ID15203991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:89090793..89123716hg38UCSC Ensembl
Outerchr7:88720107..88753030hg19UCSC Ensembl
Outerchr7:88558043..88590966hg18UCSC Ensembl
Outerchr7:88364758..88397681hg17UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg388076
hg198076
hg188076
hg178076
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv651
SamplesNA19240
Known GenesZNF804B
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)nsv5829
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