A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10707



Internal ID15542091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:49590606..49607765hg38UCSC Ensembl
OuterchrX:49355209..49372368hg19UCSC Ensembl
OuterchrX:49242153..49259315hg18UCSC Ensembl
OuterchrX:49058420..49075611hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3822041
hg1922041
hg1822041
hg1722041
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6899
Supporting Variants
SamplesNA18956
Known GenesGAGE1, GAGE2A
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)nssv10707
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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