A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1850



Internal ID15194448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:100226294..100270884hg38UCSC Ensembl
OuterchrX:99481292..99525882hg19UCSC Ensembl
OuterchrX:99367948..99412538hg18UCSC Ensembl
OuterchrX:99287437..99332027hg17UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3844591
hg1944591
hg1844591
hg1744591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7007
Supporting Variants
SamplesNA18555
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)nssv1850
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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