A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2871



Internal ID15547434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:108420137..108451578hg38UCSC Ensembl
Outerchr2:109036593..109068034hg19UCSC Ensembl
Outerchr2:108403025..108434466hg18UCSC Ensembl
Outerchr2:108495111..108526552hg17UCSC Ensembl
Cytoband2q12.3
Allele length
AssemblyAllele length
hg3831442
hg1931442
hg1831442
hg1731442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7538
SamplesNA12156
Known GenesGCC2
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)nsv2871
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