A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6372511



Internal ID9397913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:29581978..29590923hg38UCSC Ensembl
chrX:29600095..29609040hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg388946
hg198946
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676609
Supporting Variants
SamplesNA18602
Known GenesIL1RAPL1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6372511
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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