A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674153



Internal ID9593572
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 Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6566981, essv6464245, essv6280844, essv5561496, essv6359370
SamplesNA19469, NA18517, NA19457, NA19324, NA18908
Known GenesZNF804B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674153
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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