A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6395251



Internal ID9539688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:98026154..98028110hg38UCSC Ensembl
Outerchr7:98025733..98028480hg38UCSC Ensembl
Innerchr7:97655466..97657422hg19UCSC Ensembl
Outerchr7:97655045..97657792hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg382748
hg192748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662173
Supporting Variants
SamplesNA19070
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6395251
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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