A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635908



Internal ID7022705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24820390..24839871hg38UCSC Ensembl
Innerchr15:24820540..24839721hg38UCSC Ensembl
Outerchr15:24820240..24840021hg38UCSC Ensembl
chr15:25065537..25085018hg19UCSC Ensembl
Innerchr15:25065687..25084868hg19UCSC Ensembl
Outerchr15:25065387..25085168hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3819482
hg1919482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15184925, essv15184928, essv15184922, essv15184926, essv15184924, essv15184927, essv15184921, essv15184920, essv15184923
SamplesHG02628, HG02952, NA19131, NA19172, HG01312, HG03109, HG03367, HG02982, NA19248
Known GenesSNRPN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635908
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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