A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7412



Internal ID15536452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:72791835..72827632hg38UCSC Ensembl
Outerchr18:70459070..70494867hg19UCSC Ensembl
Outerchr18:68610050..68645847hg18UCSC Ensembl
Outerchr18:68610050..68645847hg17UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3835798
hg1935798
hg1835798
hg1735798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2351
Supporting Variants
SamplesNA12156
Known GenesNETO1
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)nssv7412
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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