A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9739755



Internal ID18714001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:1037152..1040192hg38UCSC Ensembl
Outerchr7:1036365..1040462hg38UCSC Ensembl
Innerchr7:1076788..1079828hg19UCSC Ensembl
Outerchr7:1076001..1080098hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg384098
hg194098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3541008
Supporting Variants
Samples
Known GenesC7orf50
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9739755
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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