A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586



Internal ID15551510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:83254913..83299897hg38UCSC Ensembl
Outerchr9:85869828..85914812hg19UCSC Ensembl
Outerchr9:85059648..85104632hg18UCSC Ensembl
Outerchr9:83099382..83144366hg17UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3844985
hg1944985
hg1844985
hg1744985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8620
SamplesNA12156
Known GenesFRMD3
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)nsv6586
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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