A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3587



Internal ID15548211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:172867810..172913078hg38UCSC Ensembl
Outerchr1:172836950..172882218hg19UCSC Ensembl
Outerchr1:171103573..171148841hg18UCSC Ensembl
Outerchr1:169568607..169613875hg17UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg3845269
hg1945269
hg1845269
hg1745269
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7825
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)nsv3587
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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