A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6425292



Internal ID9753125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:78948221..78950074hg38UCSC Ensembl
chr6:79657938..79659791hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg381854
hg191854
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675407
Supporting Variants
SamplesNA19704
Known GenesPHIP
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6425292
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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