A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661778



Internal ID9581197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:13839076..13845244hg38UCSC Ensembl
OuterchrX:13839042..13845279hg38UCSC Ensembl
InnerchrX:13857195..13863363hg19UCSC Ensembl
OuterchrX:13857161..13863398hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg386238
hg196238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5718083
SamplesNA19917
Known GenesGPM6B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661778
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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