A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675527



Internal ID9594946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:41098893..41099170hg38UCSC Ensembl
OuterchrX:41098736..41099323hg38UCSC Ensembl
InnerchrX:40958146..40958423hg19UCSC Ensembl
OuterchrX:40957989..40958576hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38588
hg19588
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6273460, essv6123481, essv6307966
SamplesNA18861, NA19461, NA18856
Known GenesUSP9X
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675527
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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