A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6302541



Internal ID9806496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:119578344..119593805hg38UCSC Ensembl
chr7:119218398..119233859hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3815462
hg1915462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2656494
Supporting Variants
SamplesNA19908
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6302541
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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