A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6368



Internal ID15190810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:120869005..120989791hg38UCSC Ensembl
OuterchrX:120002859..120123645hg19UCSC Ensembl
OuterchrX:119886887..119951326hg18UCSC Ensembl
OuterchrX:119784741..119849180hg17UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38120787
hg19120787
hg1864440
hg1764440
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7061
Supporting Variants
SamplesNA12156
Known GenesCT47A1, CT47A10, CT47A11, CT47A12, CT47A2, CT47A3, CT47A4, CT47A5, CT47A6, CT47A7, CT47A8, CT47A9, CT47B1
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)nssv6368
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