A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10153169



Internal ID154985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156331944..156348237hg38UCSC Ensembl
chr1:156301735..156318028hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg3816294
hg1916294
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3587635
Supporting Variants
SamplesHG01982
Known GenesCCT3, TSACC
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10153169
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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