A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4136



Internal ID15202129
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 StatusM
Merged Variants
Supporting Variantsnssv7899
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)nsv4136
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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