A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674329



Internal ID9593748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:109653604..109658993hg38UCSC Ensembl
chrX:108896833..108902222hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg385390
hg195390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6148730
SamplesHG01060
Known GenesACSL4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674329
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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