A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1830



Internal ID15194428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:38137694..38181944hg38UCSC Ensembl
OuterchrX:37996947..38041197hg19UCSC Ensembl
OuterchrX:37881891..37926141hg18UCSC Ensembl
OuterchrX:37753164..37797414hg17UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3844251
hg1944251
hg1844251
hg1744251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6866
Supporting Variants
SamplesNA18555
Known GenesSRPX
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)nssv1830
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