A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6867



Internal ID5089608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:38278296..38309484hg19UCSC Ensembl
OuterchrX:38163240..38194428hg18UCSC Ensembl
OuterchrX:38034513..38065701hg17UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg198686
hg188686
hg178686
Variant TypeCNV Insertion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv11212
SamplesNA15510
Known GenesOTC
Method
AnalysisSample level sites were merged to generate a set of non-redundant variant regions. Two non-redundant inversion variants (chr 2 positions 89438708-89655419 and 89958869-91208466) were corrected from the original publication for coordinates and associated sample-level data.
PlatformCapillary
Comments
ReferenceKidd et al 2008
Pubmed ID18451855
Accession Number(s)nsv6867
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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