A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3542772



Internal ID18397162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:156994381..156994505hg38UCSC Ensembl
Outerchr7:156994360..156994528hg38UCSC Ensembl
Innerchr7:156787075..156787199hg19UCSC Ensembl
Outerchr7:156787054..156787222hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9741519
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3542772
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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