A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6759



Internal ID15205014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:135565504..135598974hg38UCSC Ensembl
Outerchr9:138457350..138490820hg19UCSC Ensembl
Outerchr9:137597171..137630641hg18UCSC Ensembl
Outerchr9:135683295..135716765hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg385804
hg195804
hg185804
hg175804
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5190
SamplesNA19129
Known GenesLOC100130954, PAEP
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)nsv6759
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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