A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1842



Internal ID15541125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:67881761..67912453hg38UCSC Ensembl
OuterchrX:67101603..67132295hg19UCSC Ensembl
OuterchrX:67018328..67049020hg18UCSC Ensembl
OuterchrX:66884624..66915316hg17UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg3830693
hg1930693
hg1830693
hg1730693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6937
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)nssv1842
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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