A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6388860



Internal ID9919356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:52385173..52442179hg38UCSC Ensembl
OuterchrX:52384602..52442549hg38UCSC Ensembl
InnerchrX:52128316..52185322hg19UCSC Ensembl
OuterchrX:52127745..52185692hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3857948
hg1957948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657729
Supporting Variants
SamplesNA20818
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6388860
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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