A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6069448



Internal ID8932492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35506260..35511036hg38UCSC Ensembl
chr7:35545870..35550646hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg384777
hg194777
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674406
Supporting Variants
SamplesHG00443
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6069448
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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