A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9749637



Internal ID18377197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:92347854..92347914hg38UCSC Ensembl
chr13:93000107..93000167hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3550890
Supporting Variants
Samples
Known GenesGPC5
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9749637
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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