A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10301



Internal ID15195811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:161458809..161507103hg38UCSC Ensembl
Outerchr1:161428599..161476893hg19UCSC Ensembl
Outerchr1:159695223..159743517hg18UCSC Ensembl
Outerchr1:158241654..158289948hg17UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3848295
hg1948295
hg1848295
hg1748295
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3243
Supporting Variants
SamplesNA18956
Known GenesFCGR2A
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)nssv10301
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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