A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv622191



Internal ID15817416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:27491864..27497864hg38UCSC Ensembl
OuterchrX:27509981..27515981hg19UCSC Ensembl
OuterchrX:27419902..27425902hg18UCSC Ensembl
OuterchrX:27269638..27275638hg17UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg386001
hg196001
hg186001
hg176001
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv510530
Supporting Variants
SamplesNA10860
Known Genes
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)nssv622191
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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