A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5857501



Internal ID8834905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:119277478..119334986hg38UCSC Ensembl
OuterchrX:119277441..119335036hg38UCSC Ensembl
InnerchrX:118411441..118468949hg19UCSC Ensembl
OuterchrX:118411404..118468999hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3857596
hg1957596
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673030
Supporting Variants
SamplesNA18638
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5857501
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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