A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6537036



Internal ID9303729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:2776782..2883939hg38UCSC Ensembl
OuterchrX:2776748..2883974hg38UCSC Ensembl
InnerchrX:2694823..2801980hg19UCSC Ensembl
OuterchrX:2694789..2802015hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38107227
hg19107227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670398
Supporting Variants
SamplesNA18487
Known GenesGYG2, XG
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6537036
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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