A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757937



Internal ID18732183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:112665783..112667571hg38UCSC Ensembl
OuterchrX:112665747..112667674hg38UCSC Ensembl
InnerchrX:111909011..111910799hg19UCSC Ensembl
OuterchrX:111908975..111910902hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg381928
hg191928
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3559190
Supporting Variants
Samples
Known GenesLHFPL1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757937
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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