A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6476334



Internal ID9312499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:5443766..5445054hg38UCSC Ensembl
chrX:5361807..5363095hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg381289
hg191289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662569
Supporting Variants
SamplesNA18502
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6476334
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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