A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9756432



Internal ID18383992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:36492154..36492438hg38UCSC Ensembl
Outerchr21:36492116..36492475hg38UCSC Ensembl
Innerchr21:37864452..37864736hg19UCSC Ensembl
Outerchr21:37864414..37864773hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg38360
hg19360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3557685
Supporting Variants
Samples
Known GenesCLDN14
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9756432
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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