A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6057750



Internal ID9536666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:62229964..62230291hg38UCSC Ensembl
chr2:62457099..62457426hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2669574
Supporting Variants
SamplesNA19066
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6057750
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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