A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6679



Internal ID15551612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:114643415..114666887hg38UCSC Ensembl
Outerchr9:117405695..117429167hg19UCSC Ensembl
Outerchr9:116445516..116468988hg18UCSC Ensembl
Outerchr9:114485249..114508721hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg386554
hg196554
hg186554
hg176554
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3743
SamplesNA12878
Known GenesC9orf91, LOC100505478
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)nsv6679
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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