A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15245741



Internal ID2173182
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636430
Supporting Variants
SamplesHG01965
Known GenesFAM227B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15245741
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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