A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665763



Internal ID9931868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:41072865..41073535hg38UCSC Ensembl
chrX:40932118..40932788hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38671
hg19671
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6460042, essv5441522, essv6216042
SamplesNA19700, NA19625, HG00734
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665763
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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