A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15245738



Internal ID5247554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49359900..49397828hg38UCSC Ensembl
Innerchr15:49359900..49397828hg38UCSC Ensembl
Outerchr15:49359400..49398328hg38UCSC Ensembl
chr15:49652097..49690025hg19UCSC Ensembl
Innerchr15:49652097..49690025hg19UCSC Ensembl
Outerchr15:49651597..49690525hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3837929
hg1937929
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636427
Supporting Variants
SamplesNA18971
Known GenesFAM227B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15245738
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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