A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6571563



Internal ID9730160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:140411591..140420821hg38UCSC Ensembl
chrX:139493756..139502986hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg389231
hg199231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2676956
Supporting Variants
SamplesNA19654
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6571563
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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