A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8753



Internal ID15535111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:99164642..99209289hg38UCSC Ensembl
OuterchrX:98419640..98464287hg19UCSC Ensembl
OuterchrX:98306296..98350943hg18UCSC Ensembl
OuterchrX:98225785..98270432hg17UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3844648
hg1944648
hg1844648
hg1744648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7006
Supporting Variants
SamplesNA12156
Known Genes
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)nssv8753
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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