A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4009



Internal ID15548675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:131989006..132030618hg38UCSC Ensembl
Outerchr3:131707850..131749462hg19UCSC Ensembl
Outerchr3:133190540..133232152hg18UCSC Ensembl
Outerchr3:133190548..133232160hg17UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3841613
hg1941613
hg1841613
hg1741613
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2415
SamplesNA18555
Known GenesCPNE4
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)nsv4009
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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