A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6379412



Internal ID9798229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:69425814..69426330hg38UCSC Ensembl
Outerchr7:69425777..69426380hg38UCSC Ensembl
Innerchr7:68890800..68891316hg19UCSC Ensembl
Outerchr7:68890763..68891366hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38604
hg19604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2657945
Supporting Variants
SamplesNA19819
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6379412
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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