A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6566981



Internal ID9544384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:89048134..89049172hg38UCSC Ensembl
chr7:88677448..88678486hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg381039
hg191039
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674153
Supporting Variants
SamplesNA19457
Known GenesZNF804B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6566981
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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