A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667764



Internal ID9587183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:110738636..110741236hg38UCSC Ensembl
chrX:109981864..109984464hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg382601
hg192601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6484640
SamplesNA19009
Known GenesCHRDL1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667764
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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