A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657313



Internal ID9576732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:7249667..7250883hg38UCSC Ensembl
chrX:7167708..7168924hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg381217
hg191217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6551624
SamplesHG00284
Known GenesSTS
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657313
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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