A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3886



Internal ID15201854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:77502573..77536013hg38UCSC Ensembl
Outerchr3:77551724..77585164hg19UCSC Ensembl
Outerchr3:77634414..77667854hg18UCSC Ensembl
Outerchr3:77634414..77667854hg17UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3833441
hg1933441
hg1833441
hg1733441
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7831
SamplesNA12156
Known GenesROBO2
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)nsv3886
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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