A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6247



Internal ID15204451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:70118114..70163017hg38UCSC Ensembl
Outerchr8:71030349..71075252hg19UCSC Ensembl
Outerchr8:71192903..71237806hg18UCSC Ensembl
Outerchr8:71192903..71237806hg17UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3844904
hg1944904
hg1844904
hg1744904
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8509
SamplesNA12156
Known GenesNCOA2
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)nsv6247
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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