A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3689



Internal ID15201637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:8967425..8993205hg38UCSC Ensembl
Outerchr3:9009109..9034889hg19UCSC Ensembl
Outerchr3:8984109..9009889hg18UCSC Ensembl
Outerchr3:8984109..9009889hg17UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3825781
hg1925781
hg1825781
hg1725781
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7768
SamplesNA12156
Known GenesSRGAP3
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)nsv3689
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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