A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv896



Internal ID15198475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:103952764..104045870hg38UCSC Ensembl
OuterchrX:103207338..103300438hg19UCSC Ensembl
OuterchrX:103093994..103187094hg18UCSC Ensembl
OuterchrX:103013483..103106583hg17UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg3893107
hg1993101
hg1893101
hg1793101
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7453
Supporting Variants
SamplesNA19240
Known GenesH2BFM, H2BFWT, H2BFXP, MIR1256, TMSB15B
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)nssv896
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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