A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636427



Internal ID6676534
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15245738, essv15245737, essv15245736
SamplesNA18621, HG02128, NA18971
Known GenesFAM227B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636427
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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