A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636327



Internal ID7023121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44960767..44969245hg38UCSC Ensembl
chr15:45252965..45261443hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg388479
hg198479
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15233715, essv15233713, essv15233716, essv15233714, essv15233710, essv15233717, essv15233711, essv15233712
SamplesHG03163, NA19137, NA19235, HG03195, NA19200, NA19184, HG02577, NA12890
Known GenesC15orf43
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636327
Frequency
Sample Size2504
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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