A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12182906



Internal ID5111002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6603300..6729633hg38UCSC Ensembl
chr6:6603533..6729866hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38126334
hg19126334
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3607998
Supporting Variants
SamplesNA18559
Known GenesLY86, LY86-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12182906
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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