A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5968992



Internal ID9462559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75565843..75567777hg38UCSC Ensembl
chr7:75195147..75197081hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg381935
hg191935
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674202
Supporting Variants
SamplesNA18916
Known GenesHIP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5968992
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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