A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10982



Internal ID15539570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:82571417..82601939hg38UCSC Ensembl
Outerchr17:80529293..80559815hg19UCSC Ensembl
Outerchr17:78122582..78153104hg18UCSC Ensembl
Outerchr17:78122582..78153104hg17UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg389362
hg199362
hg189362
hg179362
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2167
Supporting Variants
SamplesNA15510
Known GenesFOXK2
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)nssv10982
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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