A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9740666



Internal ID18714912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:75728684..75736682hg38UCSC Ensembl
Outerchr7:75728630..75737682hg38UCSC Ensembl
Innerchr7:75358002..75366000hg19UCSC Ensembl
Outerchr7:75357948..75367000hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg389053
hg199053
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3541919
Supporting Variants
Samples
Known GenesHIP1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9740666
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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