A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9764740



Internal ID18738986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:94713474..94713589hg38UCSC Ensembl
Outerchr1:94713468..94713597hg38UCSC Ensembl
Innerchr1:95179030..95179145hg19UCSC Ensembl
Outerchr1:95179024..95179153hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3565993
Supporting Variants
Samples
Known GenesLINC01057
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9764740
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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