A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6511265



Internal ID8744145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:88985735..88987656hg38UCSC Ensembl
OuterchrX:88985698..88987706hg38UCSC Ensembl
InnerchrX:88240736..88242657hg19UCSC Ensembl
OuterchrX:88240699..88242707hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg382009
hg192009
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2660174
Supporting Variants
SamplesHG00133
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6511265
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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