A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574



Internal ID15204811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:77810172..77847257hg38UCSC Ensembl
Outerchr9:80425088..80462173hg19UCSC Ensembl
Outerchr9:79614908..79651993hg18UCSC Ensembl
Outerchr9:77654642..77691727hg17UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg3837086
hg1937086
hg1837086
hg1737086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8615
SamplesNA12156
Known GenesGNAQ
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)nsv6574
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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