A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3014901



Internal ID10687881
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 StatusM
Merged Variants
Supporting Variantsessv7284468
SamplesHuRef
Known GenesNHS
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv3014901
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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