A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3156



Internal ID15547737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:214844299..214889399hg38UCSC Ensembl
Outerchr2:215709023..215754123hg19UCSC Ensembl
Outerchr2:215417268..215462368hg18UCSC Ensembl
Outerchr2:215534529..215579629hg17UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3845101
hg1945101
hg1845101
hg1745101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7614
SamplesNA12156
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)nsv3156
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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