A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15326382



Internal ID2689720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95565341..95589267hg38UCSC Ensembl
Innerchr15:95565491..95589117hg38UCSC Ensembl
Outerchr15:95565191..95589417hg38UCSC Ensembl
chr15:96108570..96132496hg19UCSC Ensembl
Innerchr15:96108720..96132346hg19UCSC Ensembl
Outerchr15:96108420..96132646hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3823927
hg1923927
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637338
Supporting Variants
SamplesHG02382
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15326382
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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