A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9758028



Internal ID18732274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:123238823..123239558hg38UCSC Ensembl
OuterchrX:123238686..123239635hg38UCSC Ensembl
InnerchrX:122372674..122373409hg19UCSC Ensembl
OuterchrX:122372537..122373486hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38950
hg19950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3559281
Supporting Variants
Samples
Known GenesGRIA3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9758028
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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