A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657483



Internal ID9576902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:151260933..151264576hg38UCSC Ensembl
Outerchr6:151260896..151264626hg38UCSC Ensembl
Innerchr6:151582068..151585711hg19UCSC Ensembl
Outerchr6:151582031..151585761hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg383731
hg193731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1163e199
Supporting Variantsessv6125443
SamplesHG01051
Known GenesAKAP12
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657483
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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