A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9864779



Internal ID3125458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16020256..16041292hg38UCSC Ensembl
chr1:16346751..16367787hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3821037
hg1921037
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3585326
Supporting Variants
SamplesHG02756
Known GenesCLCNKA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv9864779
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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