A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4122



Internal ID15548800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:173946146..173990357hg38UCSC Ensembl
Outerchr3:173663936..173708147hg19UCSC Ensembl
Outerchr3:175146630..175190841hg18UCSC Ensembl
Outerchr3:175146638..175190849hg17UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3844212
hg1944212
hg1844212
hg1744212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2430
SamplesNA18555
Known GenesNLGN1
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)nsv4122
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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