A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5728004



Internal ID9715110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:70903139..70904080hg38UCSC Ensembl
chrX:70122989..70123930hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38942
hg19942
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2667978
Supporting Variants
SamplesNA19467
Known GenesTEX11
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5728004
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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