A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9750992



Internal ID18725238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9249728..9249779hg38UCSC Ensembl
chr2:9389857..9389908hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3552245
Supporting Variants
Samples
Known GenesASAP2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9750992
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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