A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8773



Internal ID15535091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:123375958..123409398hg38UCSC Ensembl
OuterchrX:122509809..122543249hg19UCSC Ensembl
OuterchrX:122337490..122370930hg18UCSC Ensembl
OuterchrX:122235344..122268784hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg385994
hg195994
hg185994
hg175994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7067
Supporting Variants
SamplesNA12156
Known GenesGRIA3
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)nssv8773
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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