A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4056



Internal ID15548727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:149441396..149485702hg38UCSC Ensembl
Outerchr3:149159183..149203489hg19UCSC Ensembl
Outerchr3:150641873..150686179hg18UCSC Ensembl
Outerchr3:150641881..150686187hg17UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3844307
hg1944307
hg1844307
hg1744307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2422
SamplesNA18555
Known GenesTM4SF4
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)nsv4056
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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