A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668118



Internal ID9587537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:63269778..63275230hg38UCSC Ensembl
Outerchr2:63269735..63275280hg38UCSC Ensembl
Innerchr2:63496913..63502365hg19UCSC Ensembl
Outerchr2:63496870..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 Variantsdgv705e199
Supporting Variantsessv6421297
SamplesHG01101
Known GenesWDPCP
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668118
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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