A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664432



Internal ID9930537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:91625303..91630978hg38UCSC Ensembl
Outerchr7:91625146..91631131hg38UCSC Ensembl
Innerchr7:91254618..91260293hg19UCSC Ensembl
Outerchr7:91254461..91260446hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg385986
hg195986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5975046, essv6122041
SamplesNA19138, HG01061
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664432
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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