A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5839136



Internal ID9636005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155551519..155556252hg38UCSC Ensembl
chrX:154781180..154785913hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg384734
hg194734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665236
Supporting Variants
SamplesNA19371
Known GenesTMLHE
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5839136
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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