A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5993526



Internal ID8970929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:74963788..75064509hg38UCSC Ensembl
Outerchr7:74963417..75064879hg38UCSC Ensembl
Innerchr7:74378516..74480322hg19UCSC Ensembl
Outerchr7:74378145..74480692hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38101463
hg19102548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658348
Supporting Variants
SamplesHG00651
Known GenesWBSCR16
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5993526
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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