A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636430



Internal ID7023224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49519173..49525682hg38UCSC Ensembl
Innerchr15:49519184..49525672hg38UCSC Ensembl
Outerchr15:49519163..49525693hg38UCSC Ensembl
chr15:49811370..49817879hg19UCSC Ensembl
Innerchr15:49811381..49817869hg19UCSC Ensembl
Outerchr15:49811360..49817890hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg386510
hg196510
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15245742, essv15245741
SamplesHG01965, NA19904
Known GenesFAM227B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636430
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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