A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7284468



Internal ID10216064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:17502507..17502822hg38UCSC Ensembl
OuterchrX:17520630..17520945hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3014901
Supporting Variants
SamplesHuRef
Known GenesNHS
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7284468
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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