A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6867



Internal ID8518801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:38419043..38450231hg38UCSC Ensembl
OuterchrX:38278296..38309484hg19UCSC Ensembl
OuterchrX:38163240..38194428hg18UCSC Ensembl
OuterchrX:38034513..38065701hg17UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg388686
hg198686
hg188686
hg178686
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv11212
SamplesNA15510
Known GenesOTC
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)nsv6867
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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