A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6038563



Internal ID9147425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:65084144..65773665hg38UCSC Ensembl
chr7:64544522..65238652hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38689522
hg19694131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663227
Supporting Variants
SamplesHG01204
Known GenesCCT6P1, INTS4L2, LOC441242, SNORA22, ZNF92
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6038563
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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