A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6771



Internal ID15205028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:137412670..137444666hg38UCSC Ensembl
Outerchr9:140307122..140339118hg19UCSC Ensembl
Outerchr9:139426943..139458939hg18UCSC Ensembl
Outerchr9:137582959..137614955hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg387444
hg197444
hg187444
hg177444
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6304
SamplesNA12156
Known GenesENTPD8, EXD3, NOXA1
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)nsv6771
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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