A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7844



Internal ID15189334
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 StatusS
Merged Variantsnsv3937
Supporting Variants
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)nssv7844
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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