A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661869



Internal ID9581288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:77676985..77687039hg38UCSC Ensembl
Outerchr7:77676828..77687192hg38UCSC Ensembl
Innerchr7:77306302..77316356hg19UCSC Ensembl
Outerchr7:77306145..77316509hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3810365
hg1910365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5976862
SamplesHG00698
Known GenesRSBN1L-AS1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661869
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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