A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566



Internal ID15551488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:74253857..74288866hg38UCSC Ensembl
Outerchr9:76868773..76903782hg19UCSC Ensembl
Outerchr9:76058593..76093602hg18UCSC Ensembl
Outerchr9:74098327..74133336hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg385986
hg195986
hg185986
hg175986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv811
SamplesNA19240
Known GenesMIR6130
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)nsv6566
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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