A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2810



Internal ID15200687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:150862697..150907393hg38UCSC Ensembl
Outerchr1:150835173..150879869hg19UCSC Ensembl
Outerchr1:149101797..149146493hg18UCSC Ensembl
Outerchr1:147648246..147692942hg17UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg3844697
hg1944697
hg1844697
hg1744697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7643
SamplesNA12156
Known GenesARNT
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)nsv2810
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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