A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2834



Internal ID15547397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:96107177..96119371hg38UCSC Ensembl
Outerchr2:96772925..96785110hg19UCSC Ensembl
Outerchr2:96136652..96148837hg18UCSC Ensembl
Outerchr2:96194799..96206984hg17UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg3812195
hg1912186
hg1812186
hg1712186
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2281
SamplesNA18555
Known GenesADRA2B
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)nsv2834
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