A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11200



Internal ID15192693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:143610600..143635500hg38UCSC Ensembl
Outerchr8:144692770..144717670hg19UCSC Ensembl
Outerchr8:144763913..144788813hg18UCSC Ensembl
Outerchr8:144763913..144788813hg17UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3824901
hg1924901
hg1824901
hg1724901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6439
Supporting Variants
SamplesNA15510
Known GenesTSTA3
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)nssv11200
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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