A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570



Internal ID15204807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:76380066..76414187hg38UCSC Ensembl
Outerchr9:78994982..79029103hg19UCSC Ensembl
Outerchr9:78184802..78218923hg18UCSC Ensembl
Outerchr9:76224536..76258657hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg385316
hg195316
hg185316
hg175316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8614
SamplesNA12156
Known GenesRFK, RPSAP9
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)nsv6570
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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