A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660175



Internal ID9926280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103022987..103028730hg38UCSC Ensembl
chrX:102277915..102283658hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg385744
hg195744
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5998898, essv6100843
SamplesHG01465, HG01489
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660175
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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