A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv818



Internal ID15544696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:92752652..92786003hg38UCSC Ensembl
Outerchr9:95514934..95548285hg19UCSC Ensembl
Outerchr9:94554755..94588106hg18UCSC Ensembl
Outerchr9:92594489..92627840hg17UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg387647
hg197647
hg187647
hg177647
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6616
Supporting Variants
SamplesNA19240
Known GenesBICD2
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)nssv818
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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