A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9879



Internal ID15539954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:166739534..166771693hg38UCSC Ensembl
Outerchr4:167660685..167692844hg19UCSC Ensembl
Outerchr4:167897260..167929419hg18UCSC Ensembl
Outerchr4:168035415..168067574hg17UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3832160
hg1932160
hg1832160
hg1732160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4593
Supporting Variants
SamplesNA18507
Known GenesSPOCK3
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)nssv9879
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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