A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670582



Internal ID9936687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:16578824..16584121hg38UCSC Ensembl
OuterchrX:16578787..16584171hg38UCSC Ensembl
InnerchrX:16596947..16602244hg19UCSC Ensembl
OuterchrX:16596910..16602294hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg385385
hg195385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6290005
SamplesNA12154
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670582
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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