A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675898



Internal ID9595317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155569094..155574305hg38UCSC Ensembl
chrX:154798755..154803966hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg385212
hg195212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5830239, essv5787717, essv5420758, essv5405826, essv6507185, essv6581890, essv5759994, essv6394405, essv5489302, essv5494013
SamplesNA19445, NA19436, HG01342, HG01365, NA19463, NA19428, NA19909, NA18910, NA19235, NA19376
Known GenesTMLHE
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675898
Frequency
Sample Size1151
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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