A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5945043



Internal ID8922446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:17619311..17620044hg38UCSC Ensembl
chrX:17637431..17638164hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg38734
hg19734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2677709
Supporting Variants
SamplesNA06986
Known GenesNHS
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5945043
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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