A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10705



Internal ID15195407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:49320820..49326447hg38UCSC Ensembl
OuterchrX:49177299..49182907hg19UCSC Ensembl
OuterchrX:49064243..49069851hg18UCSC Ensembl
OuterchrX:48933670..48939278hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3822189
hg1922189
hg1822189
hg1722189
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6896
Supporting Variants
SamplesNA18956
Known GenesGAGE12J
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)nssv10705
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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