A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660140



Internal ID9579559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157401912..157402327hg38UCSC Ensembl
chr6:157822944..157823359hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38416
hg19416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6582851, essv6233476
SamplesHG00610, NA19717
Known GenesZDHHC14
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660140
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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