A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590



Internal ID15550415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:166067131..166113770hg38UCSC Ensembl
Outerchr6:166480619..166527258hg19UCSC Ensembl
Outerchr6:166400609..166447248hg18UCSC Ensembl
Outerchr6:166451030..166497669hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3846640
hg1946640
hg1846640
hg1746640
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv601
SamplesNA19240
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)nsv5590
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