A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9738689



Internal ID18712877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:71028797..71028975hg38UCSC Ensembl
Outerchr6:71028742..71029013hg38UCSC Ensembl
Innerchr6:71738500..71738678hg19UCSC Ensembl
Outerchr6:71738445..71738716hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3539942
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9738689
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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