A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5859461



Internal ID9082836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:64022455..64278986hg38UCSC Ensembl
chr7:63482833..63739364hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38256532
hg19256532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664319
Supporting Variants
SamplesHG01061
Known GenesLINC01005, ZNF679, ZNF727, ZNF735
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5859461
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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