A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6122041



Internal ID9082482
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 Flag1
Merged StatusS
Merged Variantsesv2664432
Supporting Variants
SamplesHG01061
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6122041
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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