A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664319



Internal ID9930424
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 Flag
Merged StatusM
Merged Variantsdgv1212e199
Supporting Variantsessv5859461
SamplesHG01061
Known GenesLINC01005, ZNF679, ZNF727, ZNF735
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664319
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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