A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1725



Internal ID15541008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:25113339..25150222hg38UCSC Ensembl
Outerchr8:24970854..25007737hg19UCSC Ensembl
Outerchr8:25026771..25063654hg18UCSC Ensembl
Outerchr8:25026771..25063654hg17UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3836884
hg1936884
hg1836884
hg1736884
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6123
Supporting Variants
SamplesNA18555
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)nssv1725
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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