A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5534855



Internal ID9404279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:35609325..35616279hg38UCSC Ensembl
chrX:35627442..35634396hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg386955
hg196955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668427
Supporting Variants
SamplesNA18609
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5534855
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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