A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6625



Internal ID15551553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:96959943..96994985hg38UCSC Ensembl
Outerchr9:99722225..99757267hg19UCSC Ensembl
Outerchr9:98762046..98797088hg18UCSC Ensembl
Outerchr9:96801780..96836822hg17UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg385942
hg195942
hg185942
hg175942
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv821
SamplesNA19240
Known GenesHIATL2
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)nsv6625
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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