A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2818



Internal ID15195061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:109652973..109678901hg38UCSC Ensembl
Outerchr9:112415253..112441181hg19UCSC Ensembl
Outerchr9:111455074..111481002hg18UCSC Ensembl
Outerchr9:109494808..109520736hg17UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg385669
hg195669
hg185669
hg175669
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6661
Supporting Variants
SamplesNA18555
Known GenesPALM2
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)nssv2818
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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