A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15345184



Internal ID3751250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99510839..99517472hg38UCSC Ensembl
Innerchr15:99510849..99517462hg38UCSC Ensembl
Outerchr15:99510829..99517482hg38UCSC Ensembl
chr15:100051044..100057677hg19UCSC Ensembl
Innerchr15:100051054..100057667hg19UCSC Ensembl
Outerchr15:100051034..100057687hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg386634
hg196634
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637429
Supporting Variants
SamplesHG03382
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15345184
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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