A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6651



Internal ID15204896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:104867939..104885846hg38UCSC Ensembl
Outerchr9:107630220..107648127hg19UCSC Ensembl
Outerchr9:106670041..106687948hg18UCSC Ensembl
Outerchr9:104709775..104727682hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3810681
hg1910681
hg1810681
hg1710681
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv11203
SamplesNA15510
Known GenesABCA1
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)nsv6651
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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