A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15778338



Internal ID5780154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:2747878..2774874hg38UCSC Ensembl
chr18:2747876..2774872hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3826997
hg1926997
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3641569
Supporting Variants
SamplesNA20858
Known GenesSMCHD1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15778338
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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