A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9766287



Internal ID18393847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31903724..31910723hg38UCSC Ensembl
Outerchr6:31903367..31911043hg38UCSC Ensembl
Innerchr6:31871501..31878500hg19UCSC Ensembl
Outerchr6:31871144..31878820hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg387677
hg197677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3567540
Supporting Variants
Samples
Known GenesC2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9766287
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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