A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8634



Internal ID15188544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:93013868..93047437hg38UCSC Ensembl
Outerchr9:95776150..95809719hg19UCSC Ensembl
Outerchr9:94815971..94849540hg18UCSC Ensembl
Outerchr9:92855705..92889274hg17UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg385871
hg195871
hg185871
hg175871
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617
Supporting Variants
SamplesNA12156
Known GenesFGD3
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)nssv8634
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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