A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4131



Internal ID15548810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:177648761..177681513hg38UCSC Ensembl
Outerchr3:177366549..177399301hg19UCSC Ensembl
Outerchr3:178849243..178881995hg18UCSC Ensembl
Outerchr3:178849251..178882003hg17UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3832753
hg1932753
hg1832753
hg1732753
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv352
SamplesNA19240
Known GenesLINC00578
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)nsv4131
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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