A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7899



Internal ID15189279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:178386237..178431491hg38UCSC Ensembl
Outerchr3:178104025..178149279hg19UCSC Ensembl
Outerchr3:179586719..179631973hg18UCSC Ensembl
Outerchr3:179586727..179631981hg17UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3845255
hg1945255
hg1845255
hg1745255
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4136
Supporting Variants
SamplesNA12156
Known GenesLINC01014
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)nssv7899
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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