A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635737



Internal ID7022535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20393689..20420544hg38UCSC Ensembl
chr15:20598942..20625797hg19UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3826856
hg1926856
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv430e214
Supporting Variantsessv15144868, essv15144876, essv15144863, essv15144873, essv15144862, essv15144870, essv15144867, essv15144860, essv15144861, essv15144877, essv15144865, essv15144875, essv15144871, essv15144869, essv15144872, essv15144866, essv15144864, essv15144874
SamplesNA18998, NA20339, NA21137, HG03782, HG03436, HG04106, HG01767, HG03132, NA19982, NA20903, HG02675, NA18632, HG03367, NA20357, HG02379, NA12830, HG04153, HG03698
Known GenesHERC2P3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635737
Frequency
Sample Size2504
Observed Gain18
Observed Loss0
Observed Complex0
Frequencyn/a


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