A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3559006



Internal ID18760082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:79469358..79469413hg38UCSC Ensembl
chrX:78724855..78724910hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9757753
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3559006
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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