A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7182



Internal ID15536682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:69287853..69332950hg38UCSC Ensembl
Outerchr1:69753536..69798633hg19UCSC Ensembl
Outerchr1:69526124..69571221hg18UCSC Ensembl
Outerchr1:69465557..69510654hg17UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3845098
hg1945098
hg1845098
hg1745098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1310
Supporting Variants
SamplesNA12156
Known Genes
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)nssv7182
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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