A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv510835



Internal ID15826860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:78439475..78526571hg38UCSC Ensembl
OuterchrX:77694972..77782068hg19UCSC Ensembl
OuterchrX:77581628..77668724hg18UCSC Ensembl
OuterchrX:77501117..77588213hg17UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3887097
hg1987097
hg1887097
hg1787097
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv618869
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)nsv510835
Frequency
Sample Size4
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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