A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15320966



Internal ID5322782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92496954..92603286hg38UCSC Ensembl
Innerchr15:92496966..92603275hg38UCSC Ensembl
Outerchr15:92496943..92603298hg38UCSC Ensembl
chr15:93040184..93146516hg19UCSC Ensembl
Innerchr15:93040196..93146505hg19UCSC Ensembl
Outerchr15:93040173..93146528hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38106333
hg19106333
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637263
Supporting Variants
SamplesHG01597
Known GenesC15orf32, LINC00930
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15320966
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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