A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6897



Internal ID15205166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:49328477..49333315hg38UCSC Ensembl
OuterchrX:49184957..49189793hg19UCSC Ensembl
OuterchrX:49071901..49076737hg18UCSC Ensembl
OuterchrX:48941328..48946164hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3834759
hg1934759
hg1834759
hg1734759
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1836, nssv868, nssv10706
SamplesNA18956, NA19240, NA18555
Known GenesGAGE12J, GAGE13, GAGE2E, GAGE8
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)nsv6897
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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