A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9738950



Internal ID18713196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:99586705..99587336hg38UCSC Ensembl
Outerchr6:99586551..99587505hg38UCSC Ensembl
Innerchr6:100034581..100035212hg19UCSC Ensembl
Outerchr6:100034427..100035381hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg38955
hg19955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3540203
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9738950
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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