A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3937



Internal ID15201910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:108393925..108409249hg38UCSC Ensembl
Outerchr3:108112772..108128096hg19UCSC Ensembl
Outerchr3:109595462..109610786hg18UCSC Ensembl
Outerchr3:109595462..109610786hg17UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3815325
hg1915325
hg1815325
hg1715325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7844
SamplesNA12156
Known GenesMYH15
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)nsv3937
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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