A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6056082



Internal ID8966191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1607817..1608962hg38UCSC Ensembl
chrX:1726710..1727855hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg381146
hg191146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662274
Supporting Variants
SamplesHG00536
Known GenesASMT
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6056082
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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