A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635821



Internal ID6675932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22818925..22904223hg38UCSC Ensembl
chr15:22968845..23054143hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3885299
hg1985299
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15176444, essv15176442, essv15176443
SamplesNA18507, HG02075, HG00263
Known GenesCYFIP1, NIPA1, NIPA2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635821
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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