A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv510526



Internal ID15478024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:15533479..15539479hg38UCSC Ensembl
OuterchrX:15551602..15557602hg19UCSC Ensembl
OuterchrX:15461523..15467523hg18UCSC Ensembl
OuterchrX:15311259..15317259hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg386001
hg196001
hg186001
hg176001
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv618471, nssv621368, nssv622188, nssv624089
SamplesCHM, NA15510, NA18994, NA10860
Known GenesBMX
MethodOptical mapping
AnalysisSingle-molecule optical maps were assembled into genome-wide consensus maps. These consensus maps were compared to a restriction map generated from the NCBI b35 human genome reference sequence.
PlatformOptical Mapping
Comments
ReferenceTeague_et_al_2010
Pubmed ID20534489
Accession Number(s)nsv510526
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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