A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568



Internal ID15551490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:75580034..75611272hg38UCSC Ensembl
Outerchr9:78194950..78226188hg19UCSC Ensembl
Outerchr9:77384770..77416008hg18UCSC Ensembl
Outerchr9:75424504..75455742hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3831239
hg1931239
hg1831239
hg1731239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8613
SamplesNA12156
Known GenesMIR548H3
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)nsv6568
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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