A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7084



Internal ID15552058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:128250686..128294969hg38UCSC Ensembl
OuterchrX:127384663..127428947hg19UCSC Ensembl
OuterchrX:127212344..127256628hg18UCSC Ensembl
OuterchrX:127110198..127154482hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3844284
hg1944285
hg1844285
hg1744285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1867
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)nsv7084
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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