A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665723



Internal ID9931828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:63005884..63036965hg38UCSC Ensembl
chrX:62225354..62256435hg19UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg3831082
hg1931082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6054611, essv6567405
SamplesNA11919, HG01491
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665723
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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