A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3541878



Internal ID18396268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:71604174..71604249hg38UCSC Ensembl
chr7:71069159..71069234hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9740625
Samples
Known GenesWBSCR17
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3541878
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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