A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662226



Internal ID9928331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:65216775..65722644hg38UCSC Ensembl
chr7:64677153..65187617hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38505870
hg19510465
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1213e199
Supporting Variantsessv5420475
SamplesHG01375
Known GenesINTS4L2, LOC441242, ZNF92
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662226
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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