A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5961749



Internal ID8939152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:66151467..66155199hg38UCSC Ensembl
Outerchr7:66151430..66155249hg38UCSC Ensembl
Innerchr7:65616454..65620186hg19UCSC Ensembl
Outerchr7:65616417..65620236hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg383820
hg193820
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674673
Supporting Variants
SamplesHG00607
Known GenesCRCP
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5961749
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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