A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7003



Internal ID15551969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:98681532..98726917hg38UCSC Ensembl
OuterchrX:97936530..97981915hg19UCSC Ensembl
OuterchrX:97823186..97868571hg18UCSC Ensembl
OuterchrX:97742675..97788060hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3845386
hg1945386
hg1845386
hg1745386
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6355
SamplesNA12156
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)nsv7003
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