A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3210



Internal ID15537938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:162761865..162916944hg38UCSC Ensembl
Outerchr3:162479653..162634732hg19UCSC Ensembl
Outerchr3:163962347..164117426hg18UCSC Ensembl
Outerchr3:163962355..164117434hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38155080
hg19155080
hg18155080
hg17155080
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4093
Supporting Variants
SamplesNA12878
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)nssv3210
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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