A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15344330



Internal ID1665150
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637427
Supporting Variants
SamplesHG01527
Known GenesLRRC28
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15344330
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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