A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5789601



Internal ID8767004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:41355008..41356334hg38UCSC Ensembl
chrX:41214261..41215587hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg381327
hg191327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2671251
Supporting Variants
SamplesHG00640
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5789601
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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