A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1861



Internal ID15194459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:120957481..120989516hg38UCSC Ensembl
OuterchrX:120091335..120123370hg19UCSC Ensembl
OuterchrX:119919016..119951051hg18UCSC Ensembl
OuterchrX:119816870..119848905hg17UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3832036
hg1932036
hg1832036
hg1732036
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7061
Supporting Variants
SamplesNA18555
Known GenesCT47A1, CT47A10, CT47A11, CT47A12, CT47A2, CT47A3, CT47A4, CT47A5, CT47A6, CT47A8, CT47A9
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)nssv1861
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer