A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637427



Internal ID7024219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99280211..99281987hg38UCSC Ensembl
Innerchr15:99280244..99281955hg38UCSC Ensembl
Outerchr15:99280179..99282020hg38UCSC Ensembl
chr15:99820416..99822192hg19UCSC Ensembl
Innerchr15:99820449..99822160hg19UCSC Ensembl
Outerchr15:99820384..99822225hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg381777
hg191777
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15344330
SamplesHG01527
Known GenesLRRC28
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637427
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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