A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5666608



Internal ID9119834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1603683..1604068hg38UCSC Ensembl
chrX:1722576..1722961hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38386
hg19386
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2664463
Supporting Variants
SamplesHG01134
Known GenesASMT
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5666608
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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