A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660740



Internal ID9926845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:113931104..113931184hg38UCSC Ensembl
chrX:113174380..113174460hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6545291, essv5813126, essv6004575, essv6280645, essv5430823
SamplesNA11831, NA19257, NA18632, NA18636, HG00437
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660740
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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