A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2855



Internal ID15200732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:151963994..151993905hg38UCSC Ensembl
Outerchr1:151936470..151966381hg19UCSC Ensembl
Outerchr1:150203094..150233005hg18UCSC Ensembl
Outerchr1:148749543..148779454hg17UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3829912
hg1929912
hg1829912
hg1729912
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7664
SamplesNA12156
Known GenesS100A10
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)nsv2855
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