A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6937



Internal ID15551896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:67881761..67915990hg38UCSC Ensembl
OuterchrX:67101603..67135832hg19UCSC Ensembl
OuterchrX:67018328..67052557hg18UCSC Ensembl
OuterchrX:66884624..66918853hg17UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg3834230
hg1934230
hg1834230
hg1734230
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3796, nssv1842
SamplesNA12878, NA18555
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)nsv6937
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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