A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv866



Internal ID15198295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:49322429..49324046hg38UCSC Ensembl
OuterchrX:49178908..49180509hg19UCSC Ensembl
OuterchrX:49065852..49067453hg18UCSC Ensembl
OuterchrX:48935279..48936880hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3822228
hg1922228
hg1822228
hg1722228
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6896
Supporting Variants
SamplesNA19240
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)nssv866
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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