A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv508791



Internal ID15824818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:108769424..108777374hg38UCSC Ensembl
OuterchrX:108012654..108020604hg19UCSC Ensembl
OuterchrX:107899310..107907260hg18UCSC Ensembl
OuterchrX:107818799..107826749hg17UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg389203
hg199203
hg189203
hg179203
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv623599, nssv620954, nssv619598
SamplesNA15510, NA18994, NA10860
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)nsv508791
Frequency
Sample Size4
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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