A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636925



Internal ID7023719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75358550..75361668hg38UCSC Ensembl
Innerchr15:75358550..75361668hg38UCSC Ensembl
Outerchr15:75358297..75361858hg38UCSC Ensembl
chr15:75650891..75654009hg19UCSC Ensembl
Innerchr15:75650891..75654009hg19UCSC Ensembl
Outerchr15:75650638..75654199hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg383119
hg193119
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15293103
SamplesHG02375
Known GenesMAN2C1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636925
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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