A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv705e199



Internal ID20124007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:63269735..63275280hg38UCSC Ensembl
chr2:63496870..63502415hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg385546
hg195546
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2662902, esv2668118
SamplesHG01101
Known GenesWDPCP
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv705e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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