A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672265



Internal ID9938370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:94487969..94488271hg38UCSC Ensembl
chrX:93742968..93743270hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5650353, essv5673160, essv5814224, essv5610139, essv6423083
SamplesNA19914, NA19704, HG01080, HG01048, NA19129
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672265
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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